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Cleanroom STN1000W Series 12" Sterile Nitrile Gloves (Bulk Packed)

Cleanroom STN1000W Series 12" Sterile Nitrile Gloves (Bulk Packed)

$282.90
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SKU:
STN100xW
Availability:
7 - 10 Business Days
Shipping:
Calculated at Checkout
Quantity Option (Case):
1,000 Gloves
TechNiGlove Cleanroom STN1000W Series 12" Sterile Nitrile Gloves (Bulk Packed) — Class 100 / ISO 5 Barrier Protection, ESD-Conscious Handling and Bulk-Pack Economy
Class 100 / ISO 5 Sterile (gamma irradiated) Nitrile (latex-free) White Powder-free 12" extended cuff Microtextured fingertips Ambidextrous Bulk packed 1,000 gloves / case
Product overview
TechNiGlove STN1000W bulk packed sterile nitrile gloves are built for Class 100 / ISO Class 5 controlled environments where glove integrity, consistent handling technique, and traceability are central to contamination control. The 12" cuff supports a cleaner gowning interface, microtextured fingertips improve wet/dry grip, and sterile gamma irradiation helps align with aseptic workflows where non-sterile gloves are not acceptable.
Why customers choose STN1000W
  • Sterile (gamma irradiated) option for ISO 5 work zones, aseptic steps, and other contamination-controlled tasks where sterile gloves are required by procedure.
  • Bulk packed economy: 100 gloves per bag, 10 bags per case (1,000 gloves per case) for high-throughput programs.
  • Microtextured fingertips for controlled grip on vials, tubs, tools, fixtures, wipe folds, and lightly wetted components.
  • Powder-free nitrile (latex-free) to support latex-sensitivities and reduce powder-driven residue/particle pathways.
  • Case-level batch marking and documentation availability (CoC and sterility documentation available on request) to support investigation readiness and audit discipline.
  • Published ESD-related performance data (method dependent) for customers managing static-sensitive components and controlled handling practices.
Recommended applications
  • ISO 5 critical-zone handling where sterile gloves are required by gowning and contamination control procedures
  • Pharmaceutical activities and controlled compounding workflows (including USP <797> programs, as specified by your SOP)
  • Chemotherapy-related handling workflows (as specified by your facility program)
  • Cleanroom material transfer, staging, and set-up steps where sterile barrier protection is required
  • Industrial and laboratory contamination-controlled work environments that standardize on sterile gloves for risk reduction
Practical reminder: bulk packed sterile gloves require disciplined bag-opening and dispensing technique to avoid re-contaminating the glove surface. Many ISO 5 programs standardize a controlled “open/dispense/change” sequence and define glove-change triggers at critical steps.
Specifications (from published technical data)
SKU family STN100xW (size-specific ordering below)
Cleanroom classification Class M3.5 / Class 100 / ISO Class 5
Material / color Nitrile / White
Sterility Sterile; sterilized by gamma irradiation (AAMI/ASTM standards referenced by manufacturer)
Style Ambidextrous
Length 12" (300 mm)
Thickness 5 mil (0.005")
Grip surface Microtextured fingertips
Cuff Beaded
Tensile strength > 12.5 MPa (published)
Elongation at break > 500% (published)
Typical particle level < 3000 total particles/cm² (> 0.5 µm) (IEST-RP-CC005.2 method referenced)
Typical ionic extractables Fluoride: < 0.05 µg/cm²
Chloride: < 3.0 µg/cm²
Nitrite: < 0.05 µg/cm²
Nitrate: < 3.00 µg/cm²
Phosphate: < 0.05 µg/cm²
Sulphate: < 3.00 µg/cm²
Typical NVR (DI water) < 8.00 µg/cm²
ESD-related published data At 50–60% RH (as published):
Surface resistivity: < 1010 ohm/square (ESD-S11.11 referenced)
Static decay: < 0.5 seconds (RETS-5-003 referenced)
Note: ESD results are method- and condition-dependent. Use published data as directional and validate to your facility ESD program.
Packaging (case) 100 gloves/bag; 10 bags/case; 1,000 gloves/case
Documentation Certificate of Conformance and sterility documentation available on request; case marked with batch numbers for traceability
Published availability 7–10 business days (site listing)
Size note (site listing): Size 6 to 6.5 = X-Small; 7 to 7.5 = Small; 8 = Medium; 9 = Large; 10 = X-Large; 10.5+ = XX-Large.
Cleanroom program guidance (U.S. first, global context second)
In U.S.-based cleanroom and regulated manufacturing programs, gloves are treated as a primary contamination-control and mix-up risk at the point of use. Align glove selection and use with your quality system: defined donning/doffing technique, change frequency tied to task risk, and disciplined handling at critical steps. For common cleanroom terminology and classification alignment, ISO 14644 language is widely used in the U.S. alongside FDA expectations and internal risk-based controls. In sterile compounding, USP <797> (and USP <800> where applicable) further reinforce technique, segregation, and documented practices.
As a secondary/global benchmark, EU GMP Annex 1 reinforces contamination control strategy (CCS) thinking: risk-based control of material transfers, validated cleaning/disinfection practices, and documentation/traceability that supports investigation readiness. Use Annex 1 as a continuous improvement lens where it fits your business, without treating it as a U.S. legal requirement.
Helpful standards and guidance hubs (for program reference): https://www.iso.org/standard/53394.html  |  https://www.fda.gov  |  https://www.astm.org  |  https://www.iest.org
Build a best-in-class ISO 5 consumables set
Gloves are only one part of ISO 5 contamination control. To reduce overall particle and residue risk, many programs standardize a matching set: sterile gloves, cleanroom-appropriate wipers, and precision swabs—all selected to support controlled technique, traceability, and repeatable outcomes.
Texwipe pairing suggestion (ISO 5-aligned wiping and swabbing)
For over 35 years, SOS and Texwipe have been close partners, and SOSCleanroom is the authorized Master Distributor of ITW Texwipe for the United States market. In ISO 5 programs, customers often pair sterile glove use with proven, cleanroom-processed polyester wipers for routine wipe-down and spill control where a low-linting wipe is required (note: no wiper is truly lint-free).
  • Wipers: Texwipe AlphaWipe® TX1009 / TX1009B polyester wipers (cleanroom laundered and packaged) for general wiping and controlled solvent wipe-downs.
  • Swabs: Texwipe CleanFoam® and Alpha® swabs for precision cleaning of ports, ledges, grooves, and hard-to-reach wipe points where wipe-fold technique is not feasible (select head material and geometry to your surface and chemistry).
Explore options: AlphaWipe wipers  |  Texwipe swabs
About TechNiGlove and SOSCleanroom supply confidence
TechNiGlove specializes in gloves for cleanroom and controlled-environment use where customers need published cleanliness context, consistent performance, and documentation support. For STN1000W, the manufacturer publishes contamination-control metrics and notes manufacturing in ISO 9001:2015 and ISO 14001:2015 certified facilities (see documentation for revision-specific details).
SOSCleanroom supports customers who need dependable, best-in-class cleanroom consumables with fast shipping, excellent customer service, fair pricing, and continuity of supply backed by decades serving controlled environments. If your qualification package requires specific certificates (CoC, irradiation/sterility documentation, lot/batch traceability), contact SOSCleanroom so the right documents match your incoming inspection and release process.
Documentation
Product spec sheet (manufacturer PDF): stn200-stn1000-stn2000_FRONT.pdf
Certificate of Conformance example (manufacturer PDF): TechniGlove-141024-TN1000W.pdf
Chemical compatibility reference (manufacturer PDF): TechNiGlove_Chem_Resistance_Chart.pdf
If you have any questions please email us at Sales@SOSsupply.com or give us a call at (214)340-8574.
If you need additional information please try our SOSCleanroom specific AI ChatBot which draws from our extensive cleanroom specific libraries.
Last updated: January 10, 2026
© 2026 SOSCleanroom.com
The Technical Vault
By SOSCleanroom
TechNiGlove STN1000W Series Sterile Nitrile Gloves (Bulk Packed) — ISO 5 / Class 100, 12" Extended Cuff, Microtextured Grip + ESD-Conscious Handling
Sterile (gamma irradiated) ISO 5 / Class 100 (M3.5) Nitrile (latex-free) 12" extended cuff Bulk packed: 1,000/case Microtextured fingertips Published ESD data
1. Practical solutions in a critical environment

In ISO 5 (Class 100) work zones, gloves are not just PPE — they become a primary contamination-control surface that can either protect the process or introduce risk. The STN1000W series is positioned for routine sterile handling where teams want sterile (gamma irradiated) nitrile, a 12" cuff to support a cleaner gowning interface, and published cleanliness context to support risk-based placement.

The operational tradeoff is intentional: bulk-packed presentation improves cost control and replenishment speed, but it requires disciplined bag opening, dispensing, and change-out rules so “sterile at receipt” stays “sterile at point-of-use.”

2. What this glove is for
  • ISO 5 critical-zone handling where sterile gloves are required by gowning and contamination-control procedures
  • Aseptic staging, material transfer support, and set-up steps where sterile barrier protection is required
  • Programs that standardize on powder-free, latex-free nitrile due to allergy profile and residue control priorities
  • Static-sensitive handling environments that want directional ESD performance data as part of selection and validation planning
3. Selection rationale
  • Sterile control: Gamma-irradiated sterile presentation supports ISO 5 steps where sterile gloves are required by procedure.
  • Bulk-pack economy: 100 gloves/bag and 10 bags/case (1,000/case) supports high-throughput programs that still require sterile gloves.
  • Gowning interface: 12" extended cuff supports cleaner overlap with garment cuffs and helps reduce exposed interface risk.
  • Grip and control: Microtextured fingertips improve controlled grip on vials, tools, wipe folds, and lightly wetted components without adding powder.
  • Residue and allergy profile: Powder-free nitrile helps reduce powder-driven residue pathways and supports latex-sensitivity programs.
  • Cleanliness context: Published particle/extractables screening values help teams build risk-based placement and incoming inspection expectations.
SOSCleanroom selection philosophy
SOSCleanroom supports customers who need dependable, best-in-class cleanroom consumables. In critical environments, we do not recommend “good enough” substitutes when process risk, product integrity, and compliance expectations are on the line.
4. Materials and construction
  • Material: Nitrile
  • Color: White
  • Shape: Ambidextrous
  • Cuff: Beaded, 12" extended cuff (300 mm)
  • External surface: Microtextured fingertips
  • Internal surface: Smooth (typical for powder-free cleanroom nitrile)
  • Powder content: Powder-free
5. Specifications in context

For ISO 5 workflows, “specs” matter most when they translate into operator control: cuff length that supports gown overlap, thickness that balances durability with touch, and published cleanliness/ESD context that helps quality teams define where the glove belongs and what records to keep.

Specification Value Operational meaning
Cleanroom class Class 100 / ISO 5 (M3.5 positioning) Intended for critical-zone work where glove cleanliness characteristics and handling discipline are central to outcomes.
Sterility Sterile; gamma irradiated Supports procedures that require sterile gloves (facility-defined); maintain sterility through controlled dispense and change-out triggers.
Freedom from holes Manufacturer program documentation available on request For ISO 5 steps, define acceptable quality levels and incoming inspection expectations with QA; use lot-level documentation where required.
Length 12" (300 mm) Improves overlap with garment cuffs and reduces interface exposure risk in gowning and aseptic handling steps.
Thickness targets 5 mil (0.005") Balances tactile control with durability for routine sterile handling; validate against your task set and change-out model.
Tensile (before aging) > 12.9 MPa (published) Directional durability indicator; monitor real-world tear/puncture events and adjust change-out rules if tasks are abrasive.
Force at break (before aging) See manufacturer documentation If force-at-break is a gating spec for your program, request the current technical file and confirm revision-specific values.
Tested for chemotherapy drugs Program-dependent (confirm with facility requirements) If used in chemo-related workflows, align glove selection to your hazardous drug program and the specific test methods required by your SOP.
Anti-static Surface resistivity (in use) ~ 1×109 Ω/sq (published) Useful directional input for static-sensitive handling; validate in your ESD program at your RH and process conditions.
Country of origin See lot documentation (example CoC indicates Malaysia) If origin is a controlled attribute in purchasing, verify per lot documentation and supplier qualification file.
Shelf life See lot label / case markings Track expiration dates in inventory control; do not stage expired sterile gloves into ISO 5 areas.
6. Cleanliness metrics

In ISO 5, published cleanliness metrics are not a substitute for technique — but they help teams define where a glove belongs, what “good” looks like at receipt, and which investigations require lot documentation. Use these values as program inputs and confirm the exact revision of the manufacturer file used for your qualification package.

Metric Value Method / reference
Typical particle count ≥ 0.5 µm < 1800 total particles/cm² (> 0.5 µm) (published) IEST-RP-CC005.2 method (as published by manufacturer)
Freedom from holes Documentation available on request Confirm per supplier qualification file; align to facility acceptance criteria.

Cleanliness note: for bulk-packed sterile gloves, the most common cleanliness loss is operator-driven (handling and dispense technique). Standardize how bags are opened, how gloves are removed, and when gloves are changed.

7. Packaging, sterility, and traceability
  • Case configuration: 100 gloves/bag, 10 bags/case (1,000 gloves/case)
  • Sterilization method: Gamma irradiation
  • Available sizes: XS, S, M, L, XL, XXL (size-specific ordering under STN100xW family)
  • Shelf life: Verify on lot label / case markings
8. Best-practice use
Customer SOP disclaimer
This guidance is provided as a suggested starting point for customer SOP development and operator training. Every cleanroom and process is different. Customers must evaluate risk, validate procedures, and obtain appropriate QA/ES approval before implementation. Always follow your facility gowning and aseptic technique requirements and the manufacturer’s instructions for use.
  • Stage with intent: Stage unopened bags outside the critical zone; open the bag in a controlled location per SOP and avoid “hovering” the bag opening over critical surfaces.
  • Donning without particle events: Avoid snapping/stretching motions; seat the cuff cleanly over the garment interface and re-check fingertip seating before first critical contact.
  • Sanitization (facility-defined): If your program sanitizes gloves, use sterile alcohol and a controlled wipe technique; avoid over-wetting that can drive liquids into cuff interfaces.
  • Double-donning: Use a defined outer-glove change model for interventions; bulk-packed sterile gloves can support higher cadence change-outs when the dispense method is controlled.
  • Change-out triggers: Change immediately after any suspected breach (snag/tear), after contacting non-sterile items, after high-touch transfer events, and at defined time/step triggers in aseptic workflows.
Suggested pairings: wipers, swabs, and solutions for sterile glove workflows
In ISO 5 work, glove performance is only part of the outcome. Consistency improves when teams standardize the “glove + wiping + detailing + solution” set so operators are not improvising at point-of-use.
Use case Recommended item Why it pairs well
ISO 5 critical wipe-downs (equipment, benches, transfer items) Texwipe TX3224 Sterile TexTra10 9" x 9" Polyester Cleanroom Wiper Sterile polyester wiper for controlled wipe-fold technique and low-residue wipe-downs in critical zones.
Sterile gowning room wipe-downs and aseptic support areas Texwipe TX8932S Sterile 12" x 12" Cellulose/Polyester Cleanroom Wiper Strong blended substrate for larger wipe areas and general sterile support cleaning where absorbency and coverage matter.
Detail cleaning (ports, fittings, interfaces, corners) Texwipe STX761 Sterile Alpha® Polyester Cleanroom Swab (Long Handle) Sterile polyester swab for precision cleaning where wipe folds cannot reach; supports controlled wetting and residue removal at interfaces.
Sterile IPA delivery (routine spray application) Texwipe TX8270 Sterile 70% IPA Trigger Spray (8 oz) Ready-to-use sterile spray supports controlled application for wipe-downs and glove sanitization steps defined by SOP.
Sterile IPA bulk use (high consumption points) Texwipe TX3290 Sterile 70% IPA (1 Gallon) Bulk sterile IPA supports high-use stations; manage dispense to avoid over-wetting and cross-contamination.
Guardrail: Confirm solution compatibility with your surfaces and your facility SOPs (wet-contact time, reapplication triggers, and glove change-out triggers).
9. Common failure modes
  • Dispense contamination: Bulk-packed gloves can be re-contaminated during bag opening or glove removal if the outside bag or operator hands contact the glove exterior.
  • Over-wetting / cuff wicking: Excess alcohol can migrate toward cuff interfaces; keep wetness controlled and define reapplication triggers.
  • Pinholes / microtears during high-grip tasks: Snags on sharp edges, vial crimps, and fixtures are common; define change-out triggers for any suspected breach.
  • Technique drift during long runs: In ISO 5, the highest-risk moment is often the “routine” moment; reinforce glove change cadence and “no non-sterile contact” discipline.
  • ESD assumptions without validation: Published ESD values are condition- and method-dependent; validate in your facility ESD program at your RH and workflow conditions.
10. Other gloves to consider

These alternatives are commonly evaluated in sterile ISO 5 decision sets. Selection should be driven by allergy profile, tactile needs, and the intervention model defined in your facility procedures.

11. Program fit for regulated cleanrooms
  • ISO 5 / Class 100 areas: Sterile glove option designed for critical-zone and aseptic handling tasks where sterile gloves are required by SOP.
  • Traceability expectations: Bulk case configuration still supports lot/case-level documentation workflows when QA requires investigation readiness.
  • Static-sensitive handling: Directional ESD data is available; confirm performance in your facility program.
  • Cost-control programs: Bulk packed sterile presentation supports high-change cadence models when dispense technique is standardized and trained.
12. Source basis
Product documentation
Standards & guidance references
These references are included to support terminology and program alignment. Customers should confirm applicability to their processes and approved SOPs.
Technical Vault Notice
Important disclaimer: This entry is provided for general process support and reference only. It is not regulatory, legal, medical, or validation advice.
Customers must evaluate risk, confirm applicability to their processes, and follow their approved SOPs, QA requirements, and the manufacturer’s instructions for use.
Questions or documentation requests: Sales@SOSsupply.com  |  (214) 340-8574
Last reviewed: January 30, 2026
© 2026 SOSCleanroom.com