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Kimberly-Clark Kimtech A8 Non-Sterile Cleanroom Coveralls (Bulk Packed)

$188.84 - $229.96
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SKU:
Kimtech 4795x
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Kimberly-Clark® Kimtech™ A8 Non-Sterile Cleanroom Coveralls — Bulk Packed (25/Case)

Kimtech™ A8 cleanroom coveralls are a non-sterile, bulk-packed garment option positioned by the manufacturer for ISO Class 8 cleanroom / controlled-environment work where contamination control, coverage, and consistent gowning discipline matter. In the manufacturer’s selection guidance, A8 is aligned to bioburden-control and controlled areas commonly associated with non-sterile production, packaging, and distribution workflows.

Non-sterile note: These coveralls are not sterile. Always match garment sterility requirements to your facility SOP, product risk, and regulatory expectations.

Specifications:
  • Brand / manufacturer: Kimberly-Clark Professional™ / Kimtech™
  • Garment type: Cleanroom coverall (non-sterile)
  • Packaging: Bulk packed; manufacturer states double-bagged packaging for cleanroom handling
  • Cleanroom fit (manufacturer positioning): A8 is positioned for ISO Class 8 environments (ISO compatibility is process- and facility-dependent)
  • Key design features (manufacturer stated): lightweight, comfortable fabric; built-in thumb loops; high neck collar
  • Fit detail (manufacturer stated): two elastic bands above and below the ankle for enhanced fit/coverage
  • Case pack: 25 coveralls per case
  • Sizes / bulk-packed codes:
    • 47951 (Small) — 25/case
    • 47952 (Medium) — 25/case
    • 47953 (Large) — 25/case
    • 47954 (XL) — 25/case
    • 47955 (2XL) — 25/case
    • 47956 (3XL) — 25/case
    • 47957 (4XL) — 25/case
About the Manufacturer: 

Kimtech™ cleanroom apparel is developed for controlled environments where personnel are a primary contamination source and garment selection must support repeatable gowning habits. Manufacturer selection guidance for Kimtech™ apparel maps garment families to ISO cleanroom classes and typical controlled-environment use cases to simplify qualification planning.

 

SOSCleanroom supports contamination-control programs with dependable supply, practical selection guidance, and supporting documentation visibility for receiving and QA review.

Kimtech™ A8 Coverall Features (Manufacturer-Stated):
  • Comfortable, lightweight innovative fabric designed to move with the worker
  • Built-in thumb loops to help protect people and processes
  • High neck collar to help control contamination risk
  • Double-bagged packaging (for cleaner handling at the gowning boundary)
  • Two elastic bands above and below the ankle for enhanced fit and coverage
Benefits in a Cleanroom Program:
  • Supports glove/garment interface control: thumb loops help reduce sleeve migration and wrist exposure during work.
  • Reduces “skin-gap” risk: high neck collar supports better coverage in routine controlled-environment movement.
  • Cleaner handling at entry: double-bag packaging supports controlled introduction practices at the gowning boundary.
  • Operational comfort: lightweight construction supports compliance when garments must be worn for extended periods.
Common Applications (Manufacturer-Listed):
  • Non-sterile pharmaceutical manufacturing
  • Bio-medical research
  • Pharmaceutical compounding
  • Biotechnology
Best-Practice Use (High-Level):
  • Follow your SOP first: facility SOP governs donning order, glove strategy, and garment disposal.
  • Touch discipline: avoid contacting the exterior of the garment; treat the outside as “critical.”
  • Use thumb loops correctly: maintain coverage at the wrist and reduce sleeve ride-up before gloving.
  • Control the ankles: confirm the ankle elastics are properly seated and not rolled to reduce exposure and drag risk.

Program note: Garments reduce contamination only when paired with disciplined gowning, controlled movement, and routine cleaning of high-touch and gowning-area surfaces.

Selection Notes (A8 vs. Other Kimtech Apparel Families):
  • A8 (this product): positioned for ISO Class 8 controlled environments and non-sterile production/packaging workflows.
  • More stringent zones: if your area requires ISO Class 7/6 or sterile apparel, select the garment family and sterility that matches your SOP and qualification plan.
  • Compatibility is facility-dependent: manufacturer guidance notes that ISO compatibility depends on equipment and cleanroom capabilities.

Manufacturer literature (reference for qualification):

Kimtech™ Scientific Products Catalog (PDF)
Kimtech™ Cleanroom Apparel Catalog (PDF)

Other Similar Products Available From SOSCleanroom.com

Quick searches (site):

Notes: Need help selecting garment families (A8 vs. higher-control options), sizing, or building a gowning kit around your ISO class and workflow? Contact SOSCleanroom for practical guidance.

If you need additional information please try our SOSCleanroom specific AI ChatBot which draws from our extensive cleanroom specific libraries.

Product page updated: Jan. 13, 2026 (SOS Technical Staff)

© 2026 SOS Supply. All rights reserved.

The Technical Vault
By SOSCleanroom
Kimtech™ A8 Non-Sterile Coverall Bulk Packed (25/Case) ISO Class 8 Positioning Thumb Loops High Neck Collar Double-Bagged
Kimtech™ A8 Non-Sterile Cleanroom Coveralls — bulk-packed coverage for ISO-classified controlled environments (with ISO-first gowning guidance)
What this garment is (and what it is not)

Kimtech™ A8 coveralls are a non-sterile cleanroom garment option supplied in bulk-packed cases. The manufacturer positions the A8 family for ISO Class 8 controlled environments and bioburden-control areas associated with non-sterile production, packaging, and distribution workflows. These coveralls are designed to support contamination control through full-body coverage and practical features that help reduce exposed skin and sleeve migration during work.

Where garments fit in ISO-classified environments (ISO-first)

Cleanrooms are typically classified using the ISO 14644 series. ISO 14644-1 defines cleanroom classification in terms of airborne particle concentration limits. In practice, garments are part of the operational controls that help facilities maintain their intended cleanliness level, because people are a primary contamination source.

ISO 14644-5 (Operations) addresses operational discipline (including personnel management and entry/exit practices) that supports maintaining cleanliness during use. In other words: selecting an appropriate garment is important, but gowning technique and behavior are usually the make-or-break variables.

Manufacturer-stated configuration, features, and ordering (bulk pack)

The table below consolidates the manufacturer’s bulk-packed A8 coverall codes and case quantities for receiving and qualification planning.

Bulk code Size Total / case
47951Small25
47952Medium25
47953Large25
47954XL25
479552XL25
479563XL25
479574XL25
Manufacturer-stated feature highlights
  • Comfortable, lightweight innovative fabric designed to move with the worker.
  • Built-in thumb loops to help protect people and processes.
  • High neck collar to help control contamination risk.
  • Double-bagged packaging for cleanroom handling practices.
  • Two elastic bands above and below the ankle for enhanced fit and coverage.
Cleanroom gowning (donning) guidance to minimize contamination (ISO-first)

Context: ISO classification (ISO 14644-1) tells you the airborne cleanliness target; operations guidance (ISO 14644-5) addresses the behaviors and controls that help you maintain it. Gowning is one of the highest-impact controls because it reduces particle and fiber shedding from skin and clothing into the environment.

A practical, SOP-friendly donning sequence (use your facility SOP as the authority)
  1. Pre-entry checks: remove exposed personal items (watches/jewelry), confirm correct size, and inspect the garment for damage.
  2. Hand hygiene: wash/sanitize per SOP before touching any cleanroom garments.
  3. Head/face coverage first: apply hair/beard cover and face mask as required by your gowning level to reduce shedding during remaining steps.
  4. Don the coverall with touch discipline: keep hands on interior surfaces as much as possible; avoid contacting the garment exterior.
  5. Secure ankles and closures: confirm ankle elastics are properly seated; close zipper/flap per garment design.
  6. Use thumb loops as intended: keep sleeves controlled and wrists covered prior to final glove placement.
  7. Glove interface control: apply gloves per SOP and confirm overlap at the cuff (many programs require a secure glove-to-sleeve interface).

Why this matters: the most common gowning contamination errors are exterior-touch events (hands contacting the outside of the suit), exposed wrist/forearm due to sleeve migration, and uncontrolled movement after gowning. Features like thumb loops and a higher collar help, but technique and training are the drivers.

European EU GMP Annex 1 considerations (added layer for sterile medicinal manufacture)

If you operate under EU GMP Annex 1 expectations (sterile medicinal products), gowning is treated as a controlled, qualified activity. Annex 1 emphasizes structured personnel controls such as separate changing rooms for different cleanroom grades and the use of airlocks, plus routine gowning qualification and periodic assessment.

Annex 1 operational takeaways (high level)
  • Maintain appropriate changing room design and grade separation (including airlocks) to prevent contamination carryover.
  • Train gowning as a formal process, qualify it, and reassess it periodically (especially for Grade A/B areas).
  • Restrict access to higher-grade areas to appropriately qualified, trained personnel.
Common gowning failure modes (and how to prevent them)
  • Touching the garment exterior while donning: keep hands on interior surfaces; slow down at the zipper/closure step.
  • Sleeves riding up / exposed wrists: use thumb loops correctly and confirm glove overlap at the cuff.
  • Ankle gaps or drag events: confirm ankle elastics are seated; avoid stepping on cuffs; move deliberately.
  • Contaminating a “clean” zone with a “dirty” touch: keep gowning rooms organized; do not set garments on non-controlled surfaces.
  • Complacency after gowning: reduce unnecessary movement; avoid leaning; maintain awareness of high-shedding behaviors.
Recommended companion items (to strengthen the program)
  • Cleanroom gloves: correct glove selection and cuff overlap are core to reducing skin-shed and maintaining the garment interface.
  • Low-lint cleanroom wipers (Texwipe): use for gowning-area touchpoint wipe-downs (benches, dispensers, carts) per SOP.
  • Cleanroom swabs (Texwipe): useful for detailed cleaning in crevices and equipment interfaces that traps contamination.
SOSCleanroom note about SOPs

The Technical Vault is written to help customers make informed contamination-control decisions and improve day-to-day handling technique. It is not your facility’s Standard Operating Procedure (SOP), batch record, or validation protocol.

Customers are responsible for establishing, training, and enforcing SOPs that fit their specific risks, products, equipment, cleanroom classification, and regulatory obligations. Always confirm suitability and acceptance criteria using your internal quality system and documented methods.

If you adapt any technique guidance from this entry, treat it as a starting template. Your team should review and approve the final method, then qualify it for your specific risk profile.

Source basis (manufacturer-first)
  • SOSCleanroom product page (this SKU family): https://www.soscleanroom.com/product/kimtech/kimberly-clark-kimtech-a8-non-sterile-cleanroom-coveralls-bulk-packed/
  • Manufacturer catalog (Kimtech™ Scientific Products Catalog, PDF): https://www.soscleanroom.com/content/Kimberly_Clark_PDF/2018%20Scientific%20Catalog.pdf
  • Manufacturer apparel catalog (PDF): https://www.soscleanroom.com/content/Kimberly_Clark_PDF/Kimtech_Cleanroom_Apparel_Catalog.pdf
  • ISO 14644-1 (classification context): https://www.iso.org/standard/53394.html
  • ISO 14644-5 (operations context): https://webstore.ansi.org/standards/iso/iso1464452025
  • EU GMP Annex 1 (European sterile manufacturing context): https://health.ec.europa.eu/system/files/2022-08/20220825_gmp-an1_en_0.pdf
SOSCleanroom is the source for this Technical Vault entry.
Briefed and approved by the SOSCleanroom (SOS) staff.
If you have any questions please email us at Sales@SOSsupply.com
If you need additional information please try our SOSCleanroom specific AI ChatBot which draws from our extensive cleanroom specific libraries.
Last reviewed: Jan. 13, 2026
© 2026 SOSCleanroom