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Cleanroom NSGF Series - Sterile Powder Free Class 100 Nitrile Gloves (Pair Packed)

Cleanroom NSGF Series - Sterile Powder Free Class 100 Nitrile Gloves (Pair Packed)

$345.00 - $365.00
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SKU:
NSGF
Availability:
7 - 10 Business Days
Shipping:
Calculated at Checkout
Quantity Option (Case):
200 Pairs
NSGF Series Sterile Powder-Free Nitrile Cleanroom Gloves — Class 100 / ISO 5, Pair-Packed for Aseptic Use
Sterile Class 100 / ISO 5 100% nitrile Powder-free Pair-packed Extended cuff Certificate of Sterility available
Product overview
NSGF Series sterile nitrile gloves are designed for aseptic operations in Class 100 / ISO Class 5 cleanrooms where glove-to-product contact is a critical contamination-control point. Each pair is cleanroom processed, sterilized, and pair-packed to support controlled donning and transfer into critical areas. The powder-free 100% nitrile formulation supports facilities managing latex sensitivities while maintaining low particle and extractables performance appropriate for sterile manufacturing and compounding environments.
Why customers choose NSGF Series
  • Sterile, ISO 5–aligned glove option for aseptic processing and critical zone operations.
  • Pair-packed configuration supports controlled transfer and clean donning technique.
  • Powder-free nitrile construction reduces residue risk and supports clean handling.
  • Extended cuff length helps maintain a secure gown–glove interface.
  • Published cleanliness and extractables data supports qualification and audit readiness.
  • Lot-specific documentation available to support sterile release and investigations.
Recommended applications
  • Aseptic filling and sterile manufacturing operations
  • USP <797> sterile compounding
  • ISO 5 laminar airflow workstations and isolators
  • Critical wipe-down and component handling
  • Sterile material transfer and staging
Specifications (from published technical data)
SKU family NSGF Series
Sterility Sterile (validated sterilization process)
Cleanroom classification Class 100 / ISO Class 5
Material 100% nitrile (no natural rubber latex)
Powder content Powder-free
Style Ambidextrous
Packaging Pair-packed, cleanroom sealed
Sizes XS – XL
Certificate of Sterility / Conformance Available on request
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Last updated: January 30, 2026
© 2026 SOSCleanroom.com
The Technical Vault
By SOSCleanroom
CT International NSGF Series Sterile Powder-Free Nitrile Cleanroom Gloves — ISO 5 / Class 100, Pair-Packed, Aseptic Donning Cuff
Sterile (gamma) ISO 5 / Class 100 100% nitrile No latex proteins Hand-specific Pair packed
1. Practical solutions in a critical environment

In ISO 5 work, glove choice drives more than barrier protection—it affects donning discipline, wipe-down consistency, and the frequency of interventions during critical tasks. The NSGF Series is built for sterile, Class 100 (ISO 5) workflows where contamination control and repeatable handling matter.

The combination of sterile (gamma) processing, hand-specific fit, and a folded cuff designed for aseptic donning helps operators avoid common glove-related contamination events (cuff grabs, over-handling, and uncontrolled packaging exposure).

2. What this glove is for
  • Aseptic setup and manipulation in ISO 5 critical zones (BSC/LAFW/isolator and sterile manufacturing touchpoints).
  • Routine sterile wipe-downs and transfer disinfection steps where sterile gloves are required by SOP.
  • Sterile component handling (parts, tools, tubing, trays) when particle control and clean handling are needed.
  • Programs avoiding latex proteins due to allergy profile, audit posture, or material standardization.
3. Selection rationale
  • ISO 5 positioning: Designed for Class 100 (ISO 5) compatible or higher controlled environments.
  • Sterility approach: Gamma irradiated sterilization with a stated minimum dose (program-aligned for sterile suites).
  • Operator control: Folded cuff supports aseptic donning and reduces handling of the exterior surface during glove placement.
  • Material standardization: 100% nitrile and no latex proteins to simplify allergy and material-control programs.
  • Strength & puncture resistance: 5 mil target thickness and published mechanical properties support durability in routine ISO 5 handling.
  • Traceability expectations: Lot traceable product positioning supports documentation-driven programs and QA review.
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: 100% nitrile
  • Color: White / bisque finish (series positioning)
  • Shape: Hand-specific
  • Cuff: Tapered, beaded cuff; folded cuff for aseptic donning
  • External surface: Bisque finish for grip
  • Internal surface: Smooth (operator comfort / controlled donning)
  • Powder content: Powder-free
5. Specifications in context

Specs only help when they map to real behaviors in the room: donning control, tear resistance during manipulations, and repeatable wipe-down technique. Use the table below to connect the NSGF’s published attributes to what operators and QA teams actually manage during ISO 5 work.

Specification Value Operational meaning
Cleanroom class Class 100 (ISO 5) compatible Intended for ISO 5 critical zones and similar controlled environments where particulate discipline is required.
Sterility Sterile; gamma irradiated (minimum dose stated by manufacturer) Supports sterile handling workflows and documentation expectations when sterile gloves are required by SOP.
Freedom from holes Leak tested; sampling per MIL-STD-105E (AQL not listed) QA can tie incoming inspection to manufacturer sampling language; request lot documentation for your records.
Length 12 in (30.5 cm) Adequate wrist coverage for typical ISO 5 gown/glove interfaces and controlled movements.
Thickness targets 5.0 mil (± 1 mil) Balances tactile control with durability for routine manipulations and wipe-down support tasks.
Tensile (before aging) 2072 psi (14 MPa) Higher tensile supports tear resistance during pulls, packaging opens, and sustained handling.
Force at break (before aging) Elongation 500% Stretch capacity helps reduce failures during donning and extended movement cycles.
Tested for chemotherapy drugs Meets or exceeds ASTM D6978-05 (per manufacturer) Relevant where chemo drug handling is part of the program; confirm your facility’s specific HD risk assessment and glove-change triggers.
Anti-static Not specified If ESD control is required, validate dissipative needs separately (electronics workflows often require an explicit ESD glove spec).
Country of origin Not specified If COO is a procurement control, request documentation prior to approval.
Shelf life Not specified Use lot labeling/expiration and FIFO; capture lot and expiry during gowning stock checks.
6. Cleanliness metrics

The manufacturer positions this series with particle and extractable testing aligned to IEST-RP-CC005 guidance for gloves used in controlled environments. For regulated programs, the actionable step is to obtain lot-level documentation (CoA/CoC as applicable to your SOP) and tie it to incoming inspection and batch records.

Metric Value Method / reference
Typical particle count ≥ 0.5 µm Request lot data (program dependent) Particle/extractable testing positioned to IEST-RP-CC005 guidance (manufacturer statement)
Freedom from holes Leak tested; sampling per MIL-STD-105E Manufacturer sampling and leak test positioning

Practical note: Even with a strong glove, the most common contamination driver is handling—how the pouch is opened, how the cuff is managed, and whether operators re-sanitize consistently after contact with non-critical surfaces.

7. Packaging, sterility, and traceability
  • Case configuration: 1 pair/pouch; 50 pairs/box; 200 pairs/case (4 boxes per case)
  • Sterilization method: Gamma irradiated (minimum dose stated by manufacturer)
  • Available sizes: 6.0 through 10.0 (size increments per series offerings)
  • Shelf life: Refer to lot label / expiration (capture in receiving and gowning stock checks)
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: Present the pair pack so the cuff and hand opening can be accessed without touching the exterior glove surface; open pouches in a consistent direction to control the exposure area.
  • Donning without particle events: Use the folded cuff to control placement; avoid snapping the cuff and avoid re-gripping the glove body once seated.
  • Sanitization (facility-defined): If your SOP requires glove sanitization, apply sterile IPA consistently (coverage + contact time) and reapply after contact with non-critical surfaces.
  • Double-donning: When used, define which layer is the “work surface” glove and establish clear change triggers for the outer glove (tears, visible soil, leaving ISO 5, or after defined task steps).
  • Change-out triggers: Replace immediately for tears, wet cuffs, compromised donning, or after any event that creates doubt (dropped items, unintended contact, or uncontrolled packaging handling).
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 TX3211 SterileWipe® LP 9" x 9" Polyester Cleanroom Wiper A sterile, low-lint polyester option that supports repeatable wipe technique in critical zones.
Sterile gowning room wipe-downs and aseptic support areas Texwipe TX3224 Sterile TexTra10™ 9" x 9" Polyester Cleanroom Wiper Sealed-edge knit polyester helps reduce lint risk during routine sterile-suite wipe-downs.
Detail cleaning (ports, fittings, interfaces, corners) Texwipe STX758B Sterile Micro Alpha® Polyester Cleanroom Swab Sterile polyester swab for controlled detailing where wipers cannot reach without over-wetting.
Sterile IPA delivery (routine spray application) Texwipe TX8270 Sterile 70% IPA Trigger Spray (8 oz) Sterile, ready-to-use IPA in a trigger format supports consistent re-sanitization steps per SOP.
Sterile IPA bulk use (high consumption points) Texwipe TX3290 Sterile 70% IPA (1 gallon, 4/case) Economical sterile IPA supply for high-volume stations; validate dispensing controls to prevent over-wetting.
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
  • Over-handling during donning: Touching glove fingers/palm while seating the glove transfers particles to the work surface and defeats the purpose of controlled packaging.
  • Uncontrolled pouch opening: Ripping the pouch wide or letting the glove contact the outside packaging increases the exposed surface area and raises contamination risk.
  • Improvised sanitization: Under-wetting leads to inconsistent coverage; over-wetting can drive solvent into seams, edges, and under fixtures—use repeatable technique and defined contact time.
  • Extended wear past change triggers: Small tears and pinholes become likely after repetitive handling; define “stop and change” points for operators.
  • Missing documentation linkage: Not capturing lot/expiry (or not retaining lot docs) creates avoidable QA gaps during investigations and audits.
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
  • Sterile compounding alignment (USP workflows): Nitrile + sterile processing supports SOPs requiring sterile gloves in ISO 5 primary engineering controls and defined glove-sanitization practices.
  • Allergy and material-control posture: No latex proteins helps standardize gloves across teams and reduces allergy-driven substitutions.
  • Documentation expectations: Lot traceable positioning supports receiving controls and QA review; request lot documentation if your program requires it.
  • Contamination control strategy: Pair packing supports controlled donning and consistent staging—key drivers in operator-mediated ISO 5 work.
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