AtlasFeed Additives

Probiotics and fermentation products

Enterococcus faecium

Enterococcus faecium is a strain-specific probiotic feed additive used in animal nutrition programs to support stable digestive ecosystems, especially during feed transitions, production-stage changes, environmental stress, and formulation programs focused on gut microbial balance.

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Strain-specific Safety and efficacy depend on the exact strain
CFU-based Viable count should be guaranteed through shelf life
Stability-driven Heat, moisture, storage, and pelleting affect viability
Safety-screened AMR and virulence-factor review is essential
Enterococcus faecium feed additive visual

Product role

Where Enterococcus faecium fits

Enterococcus faecium is part of the probiotics and fermentation products group. In animal nutrition, selected feed-grade strains may be used as direct-fed microbials to support gut microbial balance, digestive resilience, feed-transition adaptation, starter-feed performance, and production-phase stability, depending on strain authorization and technical support.

This product should never be evaluated by species name alone. E. faecium is a strain-specific category where performance, safety, viable count, stability, and permitted claims depend on the exact strain, deposit number, production method, carrier, coating, storage conditions, and target species.

Atlas Feed Additives can coordinate international supplier options for feed mills, premix producers, livestock integrators, aquaculture feed producers, pet food manufacturers, distributors, and animal nutrition companies that need consistent feed-grade probiotic material with export-ready documentation.

Important safety positioning

Enterococcus faecium must be handled as a strain-specific probiotic, not as a generic microbial ingredient. Buyers should request strain identification, absence of relevant virulence factors, antimicrobial susceptibility data, absence of transferable antimicrobial resistance concerns, production-strain traceability, and market-specific authorization before use.

How it works

Live microbial support for digestive ecosystem stability

Feed-grade Enterococcus faecium products are designed to deliver viable microorganisms into the animal digestive tract. Depending on the strain and product data, they may support microbial balance, gut barrier resilience, competitive exclusion concepts, fermentation balance, feed transition management, starter-period adaptation, and performance-oriented zootechnical programs.

The practical value of a probiotic depends on viability at the point of use. Viable count can be reduced by heat, moisture, oxygen, storage time, pelleting, acids, minerals, pressure, and poor packaging. For this reason, buyers should request both initial CFU and end-of-shelf-life CFU guarantees, plus stability data under realistic feed manufacturing conditions.

  • Supports digestive ecosystem programs where the exact strain has data and authorization
  • Commonly used in starter feeds, feed-transition programs, and stress-period support strategies
  • Requires viable count verification by a suitable microbiological method
  • May be supplied as powder, coated powder, granule, soluble culture, or premix
  • Must be reviewed for strain identity, safety, antimicrobial resistance, and virulence markers

Buyer clarity

What buyers should define before comparing offers

Two Enterococcus faecium offers can be very different. One product may be a stable, documented, authorized feed strain with end-of-shelf-life CFU guarantees, while another may be a generic culture with limited strain data. Price comparison is meaningful only when strain, viable count, stability, safety documentation, and target species are aligned.

  • Exact strain designation and deposit number
  • Declared CFU/g at manufacture and at end of shelf life
  • Recommended inclusion rate and CFU delivered per animal or per kg feed
  • Species and production stage covered by authorization or supplier data
  • Pelleting, extrusion, acid, and premix stability
  • Carrier, coating, particle size, flowability, and dust level
  • Antimicrobial susceptibility and transferable resistance review
  • Virulence-factor screening and absence of relevant contaminants

Typical applications

Application areas in animal nutrition programs

Enterococcus faecium probiotic products are used in multiple animal sectors when the approved strain, viable count, inclusion rate, and product form match the species and feed process. Final use should always be aligned with local market rules and professional formulation guidance.

Poultry feed

Used in broiler, layer, breeder, and turkey programs focused on starter-feed adaptation, litter and gut-balance support, feed transition, stress-period support, and antibiotic-reduction strategies where legally permitted. Buyers should review pelleting stability, CFU recovery, and compatibility with coccidiostats, acids, enzymes, and minerals.

Swine feed

Used in piglet, nursery, grower-finisher, sow, and gilt diets where digestive stability and feed-transition resilience are priorities. Piglet programs often review viable count delivery, acidifier compatibility, pelleting tolerance, post-weaning feed intake, and strain-specific support.

Ruminant feed

Used in calf starters, milk replacer systems where suitable, dairy concentrates, mineral feeds, and specialty supplements. Ruminant buyers should review target animal age, rumen or hindgut objective, mineral-feed compatibility, carrier behavior, and stability in the final feed format.

Aquaculture feed

May be used in aquafeed programs where probiotic culture stability, extrusion survival, oil-coating compatibility, water stability, and species-specific authorization are confirmed. Buyers should request data for the exact species and processing conditions.

Companion animal diets

Used in pet food, treats, supplements, or digestive-support concepts where strain authorization, palatability, heat stability, viable count, and label requirements are suitable. Post-extrusion coating or protected culture formats may be needed to protect viability.

Premix and specialty blends

Used by premix manufacturers in probiotic blends, starter packages, gut-health concepts, and feed-transition products. Important parameters include flowability, carrier compatibility, dust control, moisture protection, uniformity, shelf life, and separation risk.

Claims and compliance note

Do not position Enterococcus faecium as a medicine, disease treatment, antibiotic replacement, or guaranteed performance enhancer unless the exact strain and product have the correct authorization and evidence. Product claims should be strain-specific, species-specific, and market-specific.

Specification guide

Typical technical points requested by buyers

The following table is a practical procurement guide. Exact values depend on supplier, strain, production process, carrier, coating, physical form, viable count, and destination-market requirements. Always confirm the offered specification and lot-specific certificate of analysis before ordering.

Product name Enterococcus faecium, E. faecium probiotic, direct-fed microbial, viable microbial culture, probiotic premix, or zootechnical additive depending on supplier documentation and market classification.
Microorganism identity Request full taxonomic identification, strain code, deposit number, identification method, and confirmation that the strain matches the product authorization or customer approval file.
Strain specificity Safety and efficacy are strain-specific. Do not assume data from one E. faecium strain applies to another strain without written supplier support.
Viable count Declared as CFU/g, CFU/kg, CFU per dose, or CFU per recommended inclusion level. Buyers should request values at manufacture and at end of shelf life.
Guarantee basis Confirm whether the guaranteed viable count is at production, shipment, delivery, end of shelf life, or after processing. End-of-shelf-life guarantee is often more meaningful for feed buyers.
Analytical method Common methods include plate-count methods, strain-selective enumeration, qPCR support, genetic identification, and supplier-validated microbiological assays. Confirm method suitability for premixes and finished feed.
Physical form Fine powder, granular powder, coated granule, microencapsulated culture, spray-dried culture, freeze-dried culture, soluble powder, liquid preparation, or carrier-based premix.
Carrier system Confirm carrier identity, carrier percentage, flowability, bulk density, particle size, dust level, moisture level, and compatibility with vitamins, minerals, enzymes, acids, oils, and other probiotics.
Coating or encapsulation For protected forms, request coating material, release concept, heat-stability data, acid tolerance, storage stability, and CFU recovery after feed processing.
Pelleting stability Request CFU recovery after the expected conditioning temperature, retention time, moisture, pressure, and cooling conditions. A strain may perform differently in mash, crumble, pellet, extruded, or coated feeds.
Acid and bile tolerance For digestive-use claims, buyers may request strain-specific tolerance data for gastric acid, bile salts, digestive pH, and survival under species-relevant conditions.
Storage stability Request viable count retention over time at recommended storage temperature and humidity. Probiotic viability can decline with heat, moisture, oxygen, and long storage.
Moisture and water activity Low moisture and controlled water activity support viable count stability. Request moisture limits and packaging designed to protect against humidity.
Safety screening Request absence or acceptable status for relevant virulence factors, hemolytic activity, unwanted biogenic amine concerns, production contaminants, and other safety criteria required by the destination market.
Antimicrobial resistance Request antimicrobial susceptibility profile, absence of transferable resistance concerns, vancomycin-resistance review where relevant, and compliance with destination-market safety criteria.
Purity and contaminants Request absence of Salmonella, E. coli, coliforms, Staphylococcus aureus, molds, yeasts where relevant, unwanted microbes, and contaminants according to the buyer's quality system.
Compatibility Review compatibility with organic acids, mineral premixes, choline chloride, enzymes, coccidiostats, medications where legally used, other probiotics, essential oils, mycotoxin binders, and preservatives.
Recommended inclusion Inclusion depends on strain, viable count, species, target claim, feed type, processing loss, and legal authorization. Buyers should request CFU delivered per animal per day or per kg finished feed.
Target species Confirm species authorization and data for poultry, swine, ruminants, aquaculture, companion animals, or other species. Do not assume cross-species use without documentation.
Packaging Common options may include foil bags, moisture-barrier bags, vacuum or nitrogen-flushed packs, plastic jars, drums, cartons, pails, or lined bags depending on product stability.
Storage Store sealed in a cool, dry, well-ventilated area, protected from heat, sunlight, moisture, oxygen exposure, pests, and contamination. Some products may require refrigeration or temperature-controlled logistics.
Shelf life Confirm production date, expiry or retest date, minimum viable count at end of shelf life, storage temperature, humidity requirements, and handling after opening.
Documentation Specification, COA, SDS, technical data sheet, strain identification, deposit certificate or strain declaration, viable count method, stability data, safety screening, antimicrobial susceptibility profile, contaminant statements, packaging list, shelf-life statement, and market-specific certificates.

Note: This table is procurement guidance only. Final specifications, claims, permitted uses, viable count guarantees, and inclusion rates must be verified against supplier documents, target species, feed processing conditions, and destination-market regulations.

Procurement note

Ask for the right specification before comparing prices.

Price comparisons are meaningful only when strain identity, viable count, CFU guarantee, product form, carrier, coating, pelleting stability, shelf-life stability, species authorization, safety screening, and documentation are aligned. A cheaper probiotic may cost more in practice if viability declines before use or if the delivered CFU is below the intended dose.

For sensitive products, also review storage temperature, humidity protection, transport time, compatibility with acids or minerals, mixing sequence, pelleting temperature, and whether the supplier can provide repeatable strain identity and viable-count documentation for every batch.

Recommended comparison rule

Compare offers by cost per delivered viable CFU at the point of use and by cost per ton of feed at the recommended inclusion rate, not only by price per kilogram. Include expected processing losses, storage losses, packaging quality, and end-of-shelf-life guarantee.

Related products

Bacillus subtilis Bacillus licheniformis Bacillus coagulans Lactobacillus acidophilus Lactobacillus plantarum Saccharomyces cerevisiae Yeast Cell Wall Mannan Oligosaccharides

Quality checklist

Buyer quality checklist for Enterococcus faecium

A complete quality checklist helps buyers avoid confusion between a documented feed-grade strain, a generic microbial powder, a fermentation by-product, a postbiotic, and a finished probiotic premix.

Identity and viable count

  • Full strain designation and deposit number
  • Genus, species, and strain confirmation
  • CFU/g at manufacture
  • Guaranteed CFU/g at end of shelf life
  • Enumeration method and acceptable tolerance
  • Recommended inclusion and delivered CFU

Stability and processing

  • Pelleting and conditioning stability
  • Premix and finished feed stability
  • Heat, moisture, acid, and oxygen tolerance
  • Carrier and coating technology
  • Particle size, flowability, and dust level
  • Storage temperature and humidity limits

Safety and compliance

  • Antimicrobial susceptibility profile
  • Transferable resistance review
  • Virulence-factor screening
  • Absence of pathogens and contaminants
  • Feed-grade suitability statement
  • Species and market authorization

Best RFQ practice

For faster supplier matching, send the desired strain or strain requirement, target species, required CFU/g, guaranteed CFU at use, feed type, processing conditions, destination country, order quantity, packaging preference, Incoterm, and complete documentation list.

Formulation considerations

Use the right product form for the feed process.

Enterococcus faecium products should be selected according to feed process, target species, and expected handling conditions. A product designed for mash feed may not survive pelleting, extrusion, acidified premixes, or long storage unless it is specifically stabilized for those conditions.

  • For mash feed, review mixing uniformity, segregation risk, and storage stability.
  • For pelleted feed, request CFU recovery after actual conditioning temperature and residence time.
  • For extruded feed, review post-extrusion coating or protected-culture formats.
  • For premixes, check compatibility with minerals, choline chloride, acids, enzymes, and high moisture carriers.
  • For liquid or water application, confirm solubility, water stability, dosing time, and biofilm-control procedures.
  • For pet food and aquafeed, review heat exposure, oil coating, palatability, and label requirements.

Species planning

Match the strain to the target animal and claim.

Probiotic products should be selected by strain data and species authorization. A strain used for piglets may not have the same evidence base for poultry, calves, fish, pets, or breeding animals. Buyers should request species-specific data when the product is used for performance or gut-balance claims.

  • Poultry: review starter feed, pelleting, coccidiostat compatibility, and gut-balance objectives.
  • Swine: review post-weaning transition, acidifier compatibility, and piglet feed intake objectives.
  • Ruminants: review calf starter, milk replacer, mineral-feed, and concentrate compatibility.
  • Aquaculture: review extrusion survival, water stability, and species-specific tolerance.
  • Companion animals: review pet food processing, palatability, and label declaration.
  • All species: confirm permitted use, inclusion guidance, and strain-specific claim language locally.

Probiotic program design

Use within a complete gut-health and quality-control system.

Enterococcus faecium can support a probiotic strategy, but it does not replace balanced formulation, hygiene, good raw-material quality, mycotoxin control, water quality, disease-prevention programs, biosecurity, or veterinary guidance. The best results usually come from matching the strain to a specific management challenge and using it consistently at the validated dose.

Before product approval

  • Confirm strain designation
  • Review viable-count guarantee
  • Check safety screening
  • Review species authorization
  • Verify processing stability
  • Request trial or field support

During production

  • Control mixing sequence
  • Monitor pelleting temperature
  • Avoid excessive moisture
  • Protect from incompatible additives
  • Use accurate dosing systems
  • Record batch traceability

After feed production

  • Store feed under dry conditions
  • Monitor shelf life
  • Retain samples
  • Test CFU recovery where needed
  • Track animal response
  • Review customer feedback

Regulatory and claim responsibility

Atlas Feed Additives can help collect supplier documents and coordinate quotations, but final approval for import, product registration, label claims, species use, safety acceptance, and inclusion rate must be confirmed by the buyer, importer, regulatory advisor, and qualified nutrition or veterinary team.

Documentation package

Documents commonly requested by professional buyers

Because Enterococcus faecium is a live microbial additive with strain-specific safety considerations, documentation is central to supplier approval. Buyers should request both quality documents and strain-safety documents before commercial use.

Core product documents

  • Product specification sheet
  • Lot-specific certificate of analysis
  • Safety data sheet
  • Technical data sheet
  • Recommended inclusion guidance
  • Packaging specification
  • Shelf-life and storage statement

Strain and performance support

  • Strain designation and deposit information
  • Genetic or molecular identification
  • Viable count method and CFU guarantee
  • Pelleting and storage stability data
  • Acid and bile tolerance data where relevant
  • Species-specific trial summaries where available
  • Recommended CFU delivery by species

Safety and compliance

  • Antimicrobial susceptibility profile
  • Transferable resistance review
  • Virulence-factor screening
  • Pathogen and contaminant absence
  • GMO, allergen, halal, or kosher statement if required
  • Country of origin declaration
  • Market authorization or feed-grade suitability statement

Document review before dispatch

Do not wait until customs clearance or customer intake to check probiotic documentation. Confirm strain identity, CFU guarantee, safety screening, antimicrobial resistance review, label language, and authorization status before dispatch, especially for markets with strict feed-additive registration rules.

Handling and storage

Practical handling guidance for live microbial products

Enterococcus faecium products contain viable microorganisms, so handling and storage conditions directly affect product performance. The goal is to protect viability until the product is consumed by the target animal.

Warehouse handling

Store sealed packaging on pallets, away from walls, floors, water sources, condensation, pests, direct sunlight, and non-feed chemicals. Use first-in, first-out stock rotation and keep damaged packaging isolated until quality review.

Temperature control

Follow the supplier's storage temperature. Some products are stable at room temperature, while others may require cool storage or refrigeration. Avoid hot warehouses, direct sun, and prolonged transport in high heat.

Moisture protection

Keep packaging closed until use. Moisture can reduce viability, increase caking, and affect flowability. Opened bags should be resealed and used within the supplier's recommended time.

Traceability records

Maintain lot number, production date, expiry or retest date, received quantity, released quantity, retained sample, storage condition, and customer allocation records for every batch.

Finished feed control

Production teams should record inclusion rate, product batch number, treated feed batch, processing temperature, and finished feed shelf life. If probiotic recovery is critical, finished feed CFU testing should be considered.

Logistics and packaging

Packaging options should protect viable count.

Probiotic logistics depend on product form, temperature sensitivity, moisture sensitivity, packaging barrier, shelf life, palletization, and destination-market documentation. Buyers should confirm packaging and transport conditions before shipment.

Common dry packaging Foil bags, aluminum-laminate bags, moisture-barrier bags, vacuum packs, nitrogen-flushed packs, paper bags with PE liners, jars, cartons, fiber drums, or pails depending on product stability and order size.
Liquid packaging Bottles, jerrycans, drums, or IBCs may be available for some liquid culture products, subject to stability, preservative system, temperature control, and transport classification.
Palletization Confirm pallet type, pallet dimensions, stretch wrap, corner protection, moisture protection, temperature exposure, total net weight, and total gross weight.
Label information Product name, strain, viable count, batch number, net weight, production date, expiry or retest date, storage instructions, supplier details, and feed-use labeling where applicable.
Shipment planning Confirm Incoterm, destination port, HS code support, container type, temperature-control requirement, moisture protection, pallet requirements, customs documentation, and maximum transit duration.
Sampling Buyers may request a laboratory approval sample, pre-shipment sample, retained sample, or sealed batch sample for strain confirmation, viable count, flowability, and customer approval testing.

Application objectives

Define the target before choosing the strain.

Probiotic products are not interchangeable unless the strain, target species, viable count, dose, product form, and authorization status match. Buyers should define the objective before requesting price comparisons.

Feed-transition support

Used where animals face diet changes, weaning, movement, new raw materials, starter-to-grower changes, or production-stage transitions. Review the exact strain data and delivered CFU for the target animal.

Gut microbial balance

Used in programs focused on digestive ecosystem stability. Buyers should review strain-specific evidence, safety documentation, and compatibility with acids, enzymes, botanicals, and other probiotics.

Antibiotic-reduction programs

May be used in broader nutrition programs seeking alternatives to routine antibiotic growth-promotion practices where regulations and customer policy allow. Claims must remain compliant and evidence-based.

Strain-specific evidence matters

Do not assume all Enterococcus faecium products behave the same. The strain, viable count, production method, coating technology, stability, and safety profile determine whether the product is suitable for a specific feed program.

Quotation workflow

How Atlas Feed Additives reviews Enterococcus faecium requests

Atlas Feed Additives supports buyers by matching probiotic requirements with suitable supplier options, available documentation, logistics conditions, and destination-market requirements.

  1. Define the target application. Share the target species, age or production stage, feed type, application objective, and whether the product will be used in starter feed, premix, pellet, extrusion, water application, pet food, or specialty supplement.
  2. Confirm strain and viable count needs. Tell us whether you need a specific strain, minimum CFU/g, CFU guarantee at shelf life, species authorization, deposit number, or compatibility with an existing probiotic program.
  3. Review stability and process conditions. Provide expected pelleting temperature, conditioning time, extrusion exposure, storage temperature, mineral premix conditions, acidifier use, and desired finished feed shelf life.
  4. Check documents and compliance. Atlas reviews specification, COA, SDS, strain identity, viable-count method, safety screening, antimicrobial susceptibility data, contaminant statements, shelf-life data, and optional certificates requested by the buyer.
  5. Compare commercial and logistics terms. Confirm quantity, packaging, destination, Incoterm, payment terms, lead time, palletization, freight option, temperature control, and quotation validity.
  6. Prepare supplier options. When suitable options are available, Atlas can provide pricing, specification summary, packaging details, available documents, and next steps for sample or order confirmation.

Incoming quality control

Suggested receiving checks

Feed mills, premix manufacturers, and distributors should define incoming inspection standards before shipment. The receiving plan should match the purchase contract, supplier COA, internal quality procedures, and destination-market requirements.

  • Confirm product name, strain, batch number, net weight, and packaging against documents.
  • Inspect bags, jars, drums, or cartons for moisture, leaks, tears, swelling, caking, heat exposure, pests, odor, or contamination.
  • Verify COA values against agreed viable-count and specification limits.
  • Check appearance, odor, color, flowability, dusting, and caking where relevant.
  • Confirm storage-temperature instructions and expiry date before release.
  • Retain a representative sample according to internal quality policy.
  • Store released product under stated conditions and segregate non-conforming lots.
  • Record production use by batch for traceability and inclusion-rate verification.

Risk reduction

Common procurement risks to avoid

  • Buying by species name only without confirming strain identity.
  • Comparing products only by price per kilogram instead of delivered viable CFU.
  • Ignoring end-of-shelf-life viable count guarantees.
  • Using a product in pelleted feed without pelleting-recovery data.
  • Skipping antimicrobial resistance and virulence-factor safety review.
  • Assuming one strain is authorized for all species and markets.
  • Mixing probiotics with incompatible acids, minerals, preservatives, or high-moisture carriers.
  • Failing to control heat and humidity during storage and transport.

Buyer questions

Questions to include in your inquiry

To help Atlas Feed Additives review suitable options quickly, include as many of the following details as possible in your first message.

Technical request

  • Required strain or strain type
  • Required CFU/g
  • CFU guarantee at end of shelf life
  • Powder, coated, encapsulated, soluble, or liquid form
  • Pelleting or extrusion stability requirement
  • Storage-temperature requirement
  • Species and target claim

Quality request

  • Specification requirements
  • COA requirements
  • Viable count method
  • Microbiological limits
  • Antimicrobial susceptibility requirements
  • Virulence-factor screening
  • Sample requirement

Commercial request

  • Order quantity
  • Annual demand estimate
  • Destination country and port
  • Preferred Incoterm
  • Packaging preference
  • Target delivery schedule
  • Required documents and certificates
Probiotic feed additive Direct-fed microbial Viable culture CFU guarantee Strain-specific Gut balance Starter feed Pelleting stability Encapsulated probiotic AMR screening Virulence review COA review SDS available Global sourcing

Questions

Useful answers

What is Enterococcus faecium used for in animal nutrition?

Enterococcus faecium is used as a strain-specific probiotic or direct-fed microbial in animal nutrition programs where buyers want support for digestive ecosystem stability, feed-transition adaptation, gut microbial balance, and zootechnical objectives. Use must match the approved strain, target species, inclusion level, and applicable market rules.

Why is strain identification important?

Safety, efficacy, stability, antimicrobial resistance profile, and permitted claims are strain-specific. Buyers should request strain designation, deposit number, molecular identification, and documentation showing that the exact strain is suitable for the intended animal and market.

What does CFU mean?

CFU means colony-forming units. It is the common way to express viable microbial count in probiotic products. Buyers should confirm CFU per gram at manufacture, guaranteed CFU at end of shelf life, and CFU delivered at the recommended inclusion rate.

Can Enterococcus faecium survive pelleting?

Survival depends on the strain, product form, coating, moisture, conditioning temperature, residence time, pressure, and cooling conditions. Buyers should request CFU recovery data under their expected feed processing conditions.

Is Enterococcus faecium suitable for all animal species?

No. Suitability depends on the exact strain, local authorization, target species, animal age, feed type, inclusion level, and claim. Buyers should confirm species-specific use with supplier documentation and qualified nutrition or regulatory support.

What safety documents should buyers request?

Buyers should request antimicrobial susceptibility profile, absence of transferable resistance concerns, virulence-factor screening, hemolysis information where relevant, strain identification, absence of contaminants, and feed-grade suitability documents required by the destination market.

How should Enterococcus faecium be stored?

Store in sealed packaging in a cool, dry, well-ventilated warehouse. Protect from heat, moisture, sunlight, oxygen exposure, pests, and contamination. Some products may require refrigeration or temperature-controlled logistics. Always follow supplier storage instructions.

Can it be mixed with acids, minerals, enzymes, or other additives?

Compatibility depends on strain, coating, carrier, moisture, pH, and storage time. Organic acids, minerals, choline chloride, preservatives, and high-moisture carriers may reduce viability in some products, so compatibility data should be requested.

What information is needed for a quotation?

Send the target species, desired strain, required CFU/g, product form, feed type, processing conditions, quantity, destination, packaging preference, Incoterm, delivery timing, storage requirement, and required documents.

Can Atlas Feed Additives quote Enterococcus faecium?

Yes. Send your required strain, viable count, target species, product form, quantity, destination, packaging preference, Incoterm, target delivery timing, and required documents so Atlas Feed Additives can review suitable supplier options for Enterococcus faecium.

Request a quotation

Tell us what you need

Send your product list, target strain, required viable count, target species, feed type, processing conditions, destination country, packaging preference, quantity, Incoterm, storage requirement, and required documents. Our team will review your request and respond from orders@feedgradeadditives.com.

orders@feedgradeadditives.com +90 507 856 26 11 WhatsApp

Helpful message example

Please quote Enterococcus faecium for feed use. Target species: broiler / piglet / calf / aquaculture / pet food. Required CFU: please offer available options. Product form: powder, coated granule, microencapsulated culture, or soluble powder. Processing: mash, pellet, extrusion, premix, or post-pellet application. Quantity: 500 kg trial order or 1 FCL. Destination: CIF Mersin / or your destination. Required documents: COA, SDS, specification, strain ID, viable-count method, stability data, safety screening, antimicrobial susceptibility profile, shelf-life statement, and feed-grade suitability statement.

Before sending your inquiry

If your request involves a specific species, claim, or regulatory market, include the destination country and intended label language. This helps review whether the strain, viable count, and documentation match local feed-additive requirements.