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Ansell 93-700 TouchNTuff Sterile Disposable Nitrile Cleanroom Gloves Class 100 (ISO 5)

Ansell 93-700 TouchNTuff Sterile Disposable Nitrile Cleanroom Gloves Class 100 (ISO 5)

$447.50
SKU: 93-700 7 - 10 Business Days
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Ansell TouchNTuff 93-700 Sterile Nitrile Cleanroom Gloves - ISO 5 / 200 Pairs

Ansell TouchNTuff 93-700 is a sterile, powder-free nitrile cleanroom glove with a nominal 300 mm extended cuff, textured fingers and an ambidextrous design. The green glove is packaged in pairs for controlled presentation. Manufacturer documentation identifies gamma sterilization to a sterility assurance level of 10-6 and positions the product for ISO Class 5 cleanroom use.

Selection focus: Match sterile status, cleanroom introduction, chemical exposure and donning requirements separately. A sterile packaged glove remains dependent on package integrity, expiry control and the facility aseptic handling procedure.

Specifications

  • Manufacturer / model: Ansell / TouchNTuff 93-700
  • Material / color: Nitrile / green; silicone-free
  • Sterility: Gamma irradiated; manufacturer SAL 10-6
  • Cleanroom positioning: Manufacturer ISO Class 5 / Class 100
  • Design / surface: Ambidextrous; textured fingers; powder-free chlorinated interior
  • Length / cuff: 300 mm nominal / 12 in; extended beaded cuff
  • Typical palm thickness: 0.13 mm / 5.1 mil
  • Typical finger thickness: 0.17 mm / 6.7 mil, per current manufacturer webpage
  • AQL for holes: 1.5
  • Manufacturer sizes: XS-XL
  • Packaging: 1 pair/wallet and sealed envelope; 10 pairs/outer bag; 5 outer bags/master bag; 4 master bags/carton = 200 pairs/carton

Where 93-700 Fits

Consider 93-700 for cleanroom workflows requiring the documented sterile presentation and extended cuff. The ISO classification describes the manufacturer use positioning, not automatic approval of every task in that room. Evaluate glove/gown overlap, aseptic donning, contamination limits and the actual chemicals or drugs handled within the facility quality system.

About the Manufacturer

Ansell publishes this model within TouchNTuff and provides product, chemical and conformity documentation for selection. Keep the exact 93-700 style and lot documents tied to the approved process instead of treating all sterile nitrile gloves as interchangeable.

Features and Practical Benefits

  • Sterile paired presentation: Supports controlled transfer and donning when packages remain intact and within their labeled use period.
  • Extended cuff: Provides additional length for assessing glove-to-gown interface coverage.
  • Textured fingers: Allow a task-specific grip evaluation while retaining an ambidextrous design.
  • Layered packaging: Enables the facility to define staged removal of outer packaging during introduction.

Common Applications

  • Aseptic and cleanroom handling under an approved facility procedure.
  • Controlled laboratory and production workflows requiring sterile gloves.
  • Chemical or drug handling only where the specific exposure and regulatory requirements have been verified.

Best-Practice Use

  1. Check model, size, lot, expiry and the integrity of the sterile envelope before introduction.
  2. Remove outer packaging at the stages required by the site transfer procedure.
  3. Don aseptically and verify the glove/gown interface; qualify fit and technique separately for single or double gloving.
  4. Replace gloves after a breach or contamination event and at the intervals established by the process.

Selection Notes and Limitations

  • Sterilization does not make a compromised or expired package acceptable.
  • AQL for holes is not a sterility assurance value; the two controls are different.
  • Chemical and chemotherapy testing is substance-specific, not universal protection.
  • A glove specification does not by itself establish compliance of an entire compounding or aseptic process.

Chemotherapy-documentation distinction: Ansell reports ASTM D6978 testing and also states that the product is not listed in US FDA 510k. Confirm the required regulatory status and drug-specific evidence before selection.

Manufacturer Documentation

Technical Vault: Open the Technical Vault tab for sterility-versus-AQL controls, aseptic packaging, chemical-test scope and chemotherapy-documentation limits.

SOSCleanroom product support: Email Sales@SOSsupply.com or call (214) 340-8574 for help confirming the model, order unit and available manufacturer documentation.

Product information reviewed: November 10, 2026
© 2026 Specialty Optical Systems, Inc. (dba SOSCleanroom). All rights reserved.

The Technical Vault

By SOSCleanroom
Sterile nitrileISO Class 5 positioningSAL 10^-6300 mm cuff200 pairs/carton

TouchNTuff 93-700: Technical Selection and Qualification

93-700 combines several independent controls: cleanroom use positioning, sterile packaging, film integrity and chemical performance. Treat those as separate acceptance criteria. An unopened sterile envelope does not establish compatibility with every chemical, while a chemical test does not validate the facility transfer or aseptic donning method.

Qualification principle: Retain lot and sterilization documentation where required, qualify package transfer and donning, and review exposure-specific data before authorizing chemical or hazardous-drug handling.

Specifications: SKU, Receiving and SOP Controls

Manufacturer / modelAnsell / TouchNTuff 93-700
Material / colorNitrile / green; silicone-free
SterilityGamma irradiated; manufacturer SAL 10-6
Cleanroom positioningManufacturer ISO Class 5 / Class 100
Design / surfaceAmbidextrous; textured fingers; powder-free chlorinated interior
Length / cuff300 mm nominal / 12 in; extended beaded cuff
Typical palm thickness0.13 mm / 5.1 mil
Typical finger thickness0.17 mm / 6.7 mil, per current manufacturer webpage
AQL for holes1.5
Manufacturer sizesXS-XL
Packaging1 pair/wallet and sealed envelope; 10 pairs/outer bag; 5 outer bags/master bag; 4 master bags/carton = 200 pairs/carton
Chemical markingManufacturer documentation: EN ISO 374-1 Type B, JKPT
Chemotherapy statementASTM D6978 testing reported; manufacturer states not listed in US FDA 510k
Case count conversion200 pairs = 400 individual gloves

Sterility, AQL and the Glove/Gown Interface

SAL 10-6 describes the manufacturer sterilization assurance claim. AQL 1.5 is a lot-sampling value for holes. They are not interchangeable and neither removes the need to check sterile packaging before use.

The 300 mm cuff provides a dimension to evaluate, not a guaranteed overlap on every gown and wearer. Include reaching, bending the wrist and routine manipulations in the qualification. For double gloving, verify both sizes and the donning sequence rather than assuming one size combination works for everyone.

Chemical and Chemotherapy Evidence

The Type B JKPT marking identifies a defined chemical-test profile. It does not authorize every solvent, disinfectant, drug concentration or contact duration. Review the specific chemical, temperature, exposure mode and relevant permeation or degradation data with the responsible safety team.

ASTM D6978 testing and US FDA listing are separate issues. This copy preserves the manufacturer qualification instead of presenting the glove as FDA-cleared for chemotherapy use. Obtain the actual drug-specific test record before deciding whether the glove meets the facility requirement.

Controlled Packaging and Quantity Verification

A full carton contains four master bags. Each master bag contains five outer bags, and each outer bag contains ten pairs. The total is 200 pairs, not 200 individual gloves. Keep the inner sterile presentation protected during storage and transfer.

  • Define the location for each packaging-removal step.
  • Do not introduce a damaged or questionable sterile envelope into the qualified workflow.
  • Keep lot and expiry identification associated with the dispensing stock after outer packaging is removed.

Receiving, Storage and Change-Out Checklist

  1. Verify 93-700, size, lot, expiry and the required sterile documentation.
  2. Confirm the case contains 200 pairs, equivalent to 400 individual gloves.
  3. Inspect all packaging levels for transport damage or loss of integrity before release.
  4. Store unopened product under the manufacturer labeled conditions and the site stock-rotation procedure.
  5. At point of use, reject damaged sterile packages and replace gloves immediately after a breach or relevant contamination event.

Technical FAQs

Does ISO Class 5 mean the glove is certified for every ISO 5 process?

No. It is manufacturer cleanroom positioning; the facility must qualify its specific process and contamination requirements.

Does SAL 10^-6 mean an opened glove remains sterile indefinitely?

No. Use depends on intact packaging, valid expiry, aseptic handling and the approved procedure.

Are 200 pairs the same as 200 gloves?

No. The carton contains 200 pairs, which is 400 individual gloves.

Is chemotherapy testing the same as US FDA 510k listing?

No. The manufacturer reports testing but expressly qualifies the US FDA listing status. Review the required documentation before use.

Why is finger thickness listed as 6.7 mil?

The current manufacturer webpage reports 0.17 mm / 6.7 mil. An older PDF contains a different mil value; the webpage value is used here with that source distinction disclosed.

Manufacturer Documentation and Source Notes

The current manufacturer webpage controls the finger-thickness value and US FDA qualification in this copy. An older PDS pairs 0.17 mm with an inconsistent mil value; that older unit entry is not carried forward. Exact exposure approval remains a facility decision.

SOSCleanroom product support: Email Sales@SOSsupply.com or call (214) 340-8574 for help confirming the model, order unit and available manufacturer documentation.

Product information reviewed: November 10, 2026
© 2026 Specialty Optical Systems, Inc. (dba SOSCleanroom). All rights reserved.