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Ansell 73-711 DermaShield Sterile Neoprene Gloves Class 100 (ISO 5)

Ansell 73-711 DermaShield Sterile Neoprene Gloves Class 100 (ISO 5)

$475.00
SKU: 73-711 7 - 10 Business Days
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Important Availability Notice: Ansell and Kimberly-Clark items, including stock items and those with 7–10 day lead times, may be delayed up to 30 days. Please contact us to confirm availability. Normal shipping is expected to resume by 1st Nov 2026

Ansell DERMASHIELD™ 73-711 Sterile Neoprene Cleanroom Gloves — Class 100 / ISO 5 Low-Allergy Protection with Textured Fingertips for Aseptic Handling
Class 100 / ISO 5 EU GMP Grade A Sterile (gamma irradiated) Neoprene (polychloroprene) Latex-free Accelerator-free Textured fingertips DERMASHIELD™ polymer coating Double-gloving friendly Chemo-tested (ASTM D6978) 12" length 200 pairs / case
Product overview
Ansell DERMASHIELD™ 73-711 is a sterile, disposable neoprene cleanroom glove built for aseptic and Class 100 / ISO 5 (EU GMP Grade A) environments where operators want a latex-free, accelerator-free barrier without giving up durability, dexterity or grip. Textured fingertips support controlled handling of components, containers and sterile packaging, while the DERMASHIELD™ internal polymer coating supports donning consistency for long shifts and double-glove programs.
Aseptic handling note
In ISO 5 work, gloves are commonly treated as the highest-frequency product-contact risk. Build glove selection into your contamination-control strategy: consistent sizing, defined change frequency, controlled donning/doffing steps, and clear “touch rules” at critical points of use.
Why customers choose DERMASHIELD™ 73-711
  • Designed for aseptic and Class 100 / ISO 5 operations where glove cleanliness, sterility and repeatable technique directly impact yield and batch integrity.
  • Latex-free and accelerator-free formulation to help reduce Type I (latex) and Type IV (chemical) sensitivity concerns in long-wear sterile programs.
  • Robust neoprene (polychloroprene) film supports puncture resistance and chemical splash protection commonly needed during cleaning and transfers.
  • Textured fingertips support secure grip during precise manipulations, especially when handling lightly wetted items or sterile pouch material.
  • Double-gloving friendly as an outer glove or underglove (define your program standard so operators do not improvise at the bench).
  • Tested for use with chemotherapy drugs in accordance with ASTM D6978 (not listed in the U.S. FDA 510(k) as published).
Recommended applications
  • Transferring liquids in controlled environments
  • Cleanroom cleaning and preparing (sterile boundary controlled steps)
  • Sample taking and processing in aseptic workflows
  • Material transfers and staging where glove integrity and documented touch discipline reduce intervention risk
  • Programs supporting hazardous drug handling where chemo-tested gloves are specified by policy (always validate to your SOP and risk assessment)
Practical technique tip: define glove-change triggers after contact with carts, door hardware, keyboards, phones, and any surface outside the controlled boundary. In ISO 5 work, “small touches” become the most common source of contamination events.
Specifications (from published technical data)
SKU 73-711
Cleanroom classification Class 100 / ISO 5 & EU GMP Grade A
Sterility / sterilization method Sterile; GAMMA irradiation (25 kGy)
Material / color Neoprene (polychloroprene) / Green
Shape Anatomic with curved fingers
Cuff Beaded with SUREFIT™ Technology (standard cuff length)
Surface / grip Textured fingertip
Internal surface Polymer coated with DERMASHIELD™ Technology
Powder content Powder-free
Typical glove length 300 mm / 12 in
Freedom from holes (AQL) 0.65 AQL
Typical particle count (cleanroom metric) ≥0.5 µm: < 3,500 counts / cm²
Thickness targets (single wall) Palm: 0.18 mm / 7.08 mil
Finger: 0.20 mm / 7.87 mil
Cuff: 0.15 mm / 5.90 mil
Double gloving recommendation Yes, as outer glove or underglove
Tested for use with chemotherapy drugs Yes, in accordance with ASTM D6978 (not listed in the U.S. FDA 510(k) as published)
Protein level N/A: contains no natural rubber latex
Anti-static No
Available sizes 6, 6.5, 7, 7.5, 8, 8.5, 9
Reorder numbers (by size) 73711060, 73711065, 73711070, 73711075, 73711080, 73711085, 73711090
Packaging (case) 200 pairs / case
1 pair per inner poly pack; 10 inner poly packs per inner polybag; 5 outer polybags per bag; 4 bags per master bag; 1 master bag of 200 pairs per carton/case
Shelf life 5 years
Storage guidance Keep out of direct sunlight; store in a cool, dry place; keep away from ozone or ignition sources.
Country of origin Sri Lanka
Quality / regulatory notes (as published) Audit standard: ISO 9001:2015
Regulatory references include: AS/NZS 4179, ASTM D3577, ASTM D7160, CE 0493, EN 556-1:2001, EN ISO 21420:2020, EN ISO 374-1:2016, EN ISO 374-5:2016, EN 421:2010, ISO 10282, ISO 11193, ISO 13485
Test method context (as published): particle metric references IEST-RP-CC005.4; thickness/length references EN 420 / ASTM D3767; AQL references EN 455-1 / ASTM D3577; chemo permeation references ASTM D6978. Always validate glove selection in your process, including disinfectant compatibility, product-contact risk, and operator technique.
Cleanroom program guidance (U.S. first, global context second)
In U.S.-based cleanrooms and regulated operations, gloves are typically treated as a primary contamination-control and mix-up risk at point of use. Many programs use ISO 14644 terminology to align cleanroom classification language, while sterile processing expectations are managed through internal quality systems and risk-based controls aligned to FDA expectations for documented training, investigations and change control. If your operation includes hazardous drug handling, ensure glove selection, double-glove rules, and change frequency are defined by policy and validated to your specific workflow (USP <800> is commonly used as a U.S. framework in applicable settings).
As a secondary/global benchmark, EU GMP Annex 1 reinforces contamination control strategy (CCS) discipline: controlled material transfers, defined glove-change triggers at critical steps, and documentation that supports traceability and 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
SOSCleanroom does not compromise on glove quality in critical environments. Ansell is positioned as a best-in-class glove line for customers who need consistent controlled-environment performance and documentation discipline. To reduce overall contamination risk in ISO 5 operations, pair sterile gloves with ISO 5-aligned wiping and swabbing materials that support controlled wetting, residue control, and repeatable technique.
Texwipe pairing suggestions (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. For ISO 5 cleaning and wipe-downs, many customers standardize on sterile 100% polyester wipers and sterile cleanroom swabs for corners, ports, threads, and detail cleaning. Where a low-linting wiper is required, remember that no wiper is truly lint-free under all process conditions.
  • Sterile wiping: Texwipe sterile AlphaWipe® polyester wipers for controlled application of disinfectants and cleaning solutions in ISO 5 workflows.
    Learn more: https://www.texwipe.com/sterile-alphawipe
  • Sterile swabbing: Texwipe CleanTips® sterile Alpha® polyester knit swabs for precision cleaning and residue removal in tight geometries (thermal bond construction to eliminate adhesive contamination; trademarked green handles and embossed Texwipe branding support authenticity and lot-level traceability at point of use).
    Learn more: https://www.texwipe.com/alpha-polyester-knit-cleanroom-swabs-sterile
  • General ISO 5 cleaning (non-sterile support areas where appropriate): Texwipe AlphaWipe® TX1009/TX1009B low-linting polyester wipers are commonly used for controlled cleaning and spill control in ISO-classified spaces (verify suitability to your area classification and SOP).
    Learn more: https://www.texwipe.com/alphawipe-tx1009
About Ansell and SOSCleanroom supply confidence
Ansell is a global manufacturer of hand and body protection solutions with controlled-environment product lines used across life sciences, critical manufacturing and laboratory settings. In cleanrooms, consistency matters: formulation control, packaging discipline and the ability to support documentation requests when customers qualify and sustain a glove program.
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. Third-party validation: Cleanroom Technology reported that SOS Cleanroom Supply became an Ansell authorised distributor (June 20, 2023): https://cleanroomtechnology.com/sos-cleanroom-supply-becomes-ansell-authorised-distributor-209576
Documentation
Product Data Sheet (PDS) – SOSCleanroom hosted (stable): dermashield-73-711_pds_us.pdf
Declaration of Conformity – SOSCleanroom hosted: DERMASHIELD™ 73-711 EU Declaration of Conformity (PDF)
UK Declaration of Conformity – SOSCleanroom hosted: DERMASHIELD™ 73-711 UK Declaration of Conformity (PDF)
Product Data Sheet (PDS) – Manufacturer hosted: Ansell PDS (DERMASHIELD™ 73-711)
Manufacturer product page: Ansell DERMASHIELD™ 73-711
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: Oct. 13, 2026
© 2026 SOSCleanroom.com
The Technical Vault By SOSCleanroom
Class 100 / ISO 5 Sterile (Gamma 25 kGy) Neoprene / Polychloroprene Latex-Free Accelerator-Free AQL 0.65 ASTM D6978 Chemo-Tested
Ansell DERMASHIELD™ 73-711: sterile neoprene cleanroom gloves for ISO 5 environments, latex-free protection, and controlled aseptic handling

Ansell DERMASHIELD™ 73-711 is a sterile, powder-free neoprene (polychloroprene) cleanroom glove designed for Class 100 / ISO Class 5 controlled environments. Its latex-free, accelerator-free formulation supports facilities managing natural rubber latex and chemical accelerator exposure concerns while maintaining the dexterity, grip, and barrier characteristics required for critical handling operations.

The glove features textured fingertips, an anatomical design with curved fingers, DERMASHIELD™ polymer-coated interior, and SUREFIT™ cuff technology. Gamma sterilization and controlled packaging support sterile gowning and material introduction procedures in aseptic environments.

Operations takeaway: DERMASHIELD™ 73-711 combines ISO 5 sterile cleanroom positioning, AQL 0.65 barrier quality, 300 mm length, and latex-free, accelerator-free construction. Its textured fingertips and beaded SUREFIT™ cuff support handling control and stable gown interfaces during routine interventions.

Chemotherapy handling consideration: DERMASHIELD™ 73-711 is identified as tested for use with chemotherapy drugs under ASTM D6978. Facilities must confirm permeation results for the specific drugs and exposure conditions involved. Testing does not establish universal protection against all chemotherapy agents.

ISO-first context: glove selection in critical cleanroom operations

ISO 14644 cleanroom operations require documented controls for personnel gowning, material transfer, cleaning, and operator behavior. In ISO 5 and other critical environments, gloves become an important contact surface between personnel, sterile materials, packaging, process equipment, and product-adjacent components.

  • Sterile processing: Gamma-sterilized gloves support aseptic handling when used within approved gowning and material-transfer procedures.
  • Particle control: Cleanroom-compatible materials and controlled glove handling help reduce contamination introduced during routine tasks.
  • Operator dexterity: Anatomically shaped fingers support repetitive manipulation of small components and sterile packaging.
  • Cuff stability: SUREFIT™ technology is designed to help maintain glove positioning and reduce cuff roll-down.
  • Exposure management: Latex-free and accelerator-free construction offers an alternative for facilities managing relevant glove-material sensitivities.

Control point: Sterile gloves can become contaminated during donning, interventions, or contact with non-controlled surfaces. Proper staging, disinfection where required, and glove-change procedures remain essential after sterile packaging is opened.

Specifications (SKU controls for RFQs, SOPs, and receiving)
  • Product: Ansell DERMASHIELD™ 73-711
  • Product type: Sterile cleanroom glove
  • Cleanroom positioning: Class 100 / ISO Class 5; EU GMP Grade A applications
  • Material: Neoprene (polychloroprene)
  • Color: Green
  • Natural rubber latex: Not made from natural rubber latex
  • Chemical accelerators: Accelerator-free
  • Powder: Powder-free
  • Sterility: Sterile
  • Sterilization method: Gamma irradiation (25 kGy)
  • Hand design: Anatomical with curved fingers
  • Exterior: Textured fingertips
  • Interior: Polymer-coated with DERMASHIELD™ Technology
  • Cuff: Beaded with SUREFIT™ Technology
  • Length: 300 mm / approximately 12 inches
  • Palm thickness: 0.18 mm / 7.08 mil
  • Finger thickness: 0.20 mm / 7.87 mil
  • Cuff thickness: 0.15 mm / 5.90 mil
  • Freedom from holes: AQL 0.65
  • Chemotherapy drug testing: ASTM D6978
  • Antistatic: No
  • Country of origin: Sri Lanka
  • Available sizes: 6, 6.5, 7, 7.5, 8, 8.5, 9
  • Shelf life: 5 years
  • Packaging: 1 pair/inner pack; 10 inner packs/inner polybag; 5 outer polybags/bag; 4 bags/master bag; 200 pairs/case

Documentation rule: Confirm current manufacturer specifications, sterilization documentation, chemotherapy permeation data, lot identification, and expiration dates before qualifying the glove for regulated sterile operations.

Performance characteristics (manufacturer-published values)
  • Cleanroom classification: Class 100 / ISO Class 5
  • Sterilization: Gamma irradiation (25 kGy)
  • Freedom-from-holes quality level: AQL 0.65
  • Glove length: 300 mm / approximately 12 inches
  • Palm thickness: 0.18 mm / 7.08 mil
  • Finger thickness: 0.20 mm / 7.87 mil
  • Cuff thickness: 0.15 mm / 5.90 mil
  • Tensile strength before aging: 17 MPa
  • Force at break before aging: 9 N
  • Typical particle count ≥ 0.5 µm: < 3,500 counts/cm²
  • Particle testing reference: IEST-RP-CC005.4
  • Freedom-from-holes testing references: EN 455-1 / ASTM D3577
  • Shelf life: 5 years

Performance interpretation: Thickness, tensile strength, particle levels, and AQL provide measurable characteristics for glove qualification. These values should be evaluated alongside the actual process, operator technique, contamination-control requirements, and chemical exposure conditions.

What DERMASHIELD™ 73-711 is designed to do (typical use cases)
  • Sterile ISO Class 5 cleanroom gowning and critical-zone operations
  • Aseptic handling and controlled interventions
  • Sterile equipment and work-surface preparation
  • Sample taking and processing in contamination-sensitive environments
  • Material transfers involving sterile packaging, components, and process equipment
  • Controlled cleaning and wipe-down procedures
  • Applications requiring a latex-free, accelerator-free sterile glove
  • Selected chemotherapy drug-handling operations where the documented ASTM D6978 permeation data and facility procedures support use
  • EU GMP Grade A sterile manufacturing applications where the glove meets facility qualification requirements

Grip-focused design: Textured fingertips, anatomical shaping, and a stable cuff support controlled handling of sterile materials, packaging, and equipment during routine processing and interventions.

Materials and construction: practical implications
  • Neoprene (polychloroprene): Provides a synthetic alternative to natural rubber latex for sterile cleanroom glove applications.
  • Accelerator-free formulation: Eliminates intentionally added chemical accelerators associated with certain glove-related contact sensitivities.
  • Powder-free construction: Removes glove powder as a potential particulate contamination pathway.
  • Anatomical design: Curved fingers support natural hand positioning during repetitive work.
  • Textured fingertips: Provide additional friction for handling containers, components, and sterile packaging.
  • DERMASHIELD™ interior: Polymer coating supports donning and helps reduce sticking during glove changes.
  • SUREFIT™ cuff: Beaded cuff design helps reduce roll-down and maintain coverage over gown interfaces.
  • Extended length: Approximately 12-inch coverage supports wrist and gown-cuff overlap.
  • Gamma sterilization: Supports sterile use when packaging integrity and aseptic handling are maintained.

Material consideration: Latex-free and accelerator-free construction can reduce exposure to these specific materials but does not eliminate every possible sensitivity or contact reaction. Facilities should evaluate individual material requirements and applicable exposure risks.

Cleanliness and contamination-control characteristics

DERMASHIELD™ 73-711 is positioned for sterile cleanroom applications where controlled particulate performance, glove integrity, and aseptic handling are important. Published values provide a basis for comparing material and contamination-control characteristics.

  • Cleanroom positioning: Class 100 / ISO Class 5
  • EU GMP application positioning: Grade A
  • Typical particle count ≥ 0.5 µm: < 3,500 counts/cm²
  • Particle testing reference: IEST-RP-CC005.4
  • Barrier integrity: AQL 0.65
  • Sterility: Gamma irradiated (25 kGy)
  • Powder: Powder-free
  • Natural rubber latex: Not made from natural rubber latex
  • Chemical accelerators: Accelerator-free
  • Antistatic performance: No

Contamination-control consideration: Sterile processing and published particle levels do not replace controlled gowning, sterile presentation, glove-disinfection procedures, and operator qualification. Actual contamination performance depends on the full process and handling method.

Packaging, sterility, and traceability
  • Individual configuration: 1 pair per inner poly pack
  • Inner polybag: 10 individually packed pairs
  • Bag: 5 outer polybags / 50 pairs
  • Master bag: 4 bags / 200 pairs
  • Carton: 1 master bag / 200 pairs per case
  • Sterilization method: Gamma irradiation (25 kGy)
  • Available sizes: 6, 6.5, 7, 7.5, 8, 8.5, 9
  • Shelf life: 5 years
  • Receiving controls: Confirm sterile packaging integrity, lot identification, product size, and expiration dating.

Procurement takeaway: Defined sterile packaging configurations help support controlled glove introduction and issuance. Maintain available lot and expiration information where required for receiving, traceability, and quality-system documentation.

Best-practice use (sterile gowning and contamination control)
  1. Verify sterile packaging: Confirm package integrity, product identification, and expiration before opening gloves for sterile use.
  2. Stage according to gowning procedures: Introduce sterile glove packs through approved material-transfer and gowning processes.
  3. Use controlled donning: Avoid snapping cuffs, excessive stretching, or unnecessary contact with glove exteriors.
  4. Maintain gown-cuff overlap: Confirm proper glove coverage over sterile garment interfaces and monitor for cuff roll-down.
  5. Protect glove integrity: Avoid sharp packaging edges, hardware corners, or handling methods that may damage the glove film.
  6. Use approved glove sanitization: Where permitted, apply facility-qualified sterile disinfectants according to defined compatibility, contact-time, and drying requirements.
  7. Double-glove when required: Follow approved inner and outer glove configurations for interventions and contamination-control procedures.
  8. Establish change-out triggers: Replace gloves after tears, punctures, cuff roll-down, visible residue, contamination, or other SOP-defined events.
  9. Control sterile handling: Minimize unnecessary packaging contact and maintain separation between sterile and non-controlled surfaces.
  10. Dispose correctly: Remove and discard gloves using approved doffing and waste-management procedures.

Method standardization tip: Define sterile glove staging, gown interface controls, disinfectant compatibility, double-gloving procedures, and replacement triggers. Consistent handling practices support repeatable contamination-control outcomes.

Recommended sterile cleanroom consumable pairings

Sterile gloves form one part of an effective contamination-control program. Pairing qualified gloves with appropriate sterile wipers, swabs, and cleaning solutions supports consistent cleaning and handling practices in ISO 5 environments.

  • Texwipe TX3224 Sterile TexTra10™ Polyester Cleanroom Wiper: A sterile 9" x 9" polyester wiper for controlled cleaning of critical surfaces. View Product
  • Texwipe TX8932S Sterile TexVantage™ Cleanroom Wiper: A sterile 12" x 12" cellulose/polyester wiper for approved gowning-room and surface cleaning applications. View Product
  • Texwipe STX763 Sterile Polyester Swab: A gamma-irradiated polyester swab for controlled detail cleaning around fittings, ports, and equipment interfaces. View Product
  • Texwipe TX8270 Sterile 70% Isopropanol: An 8 oz sterile IPA trigger spray for approved cleaning and glove-disinfection procedures. View Product
  • Texwipe TX3290 Sterile 70% Isopropanol: A 1-gallon sterile IPA option for facilities with higher-volume cleaning requirements. View Product

Compatibility consideration: Confirm that glove-disinfection procedures, cleaning solutions, wipers, and swabs meet applicable facility requirements for chemical compatibility, sterile handling, contamination control, and validation.

Misuse controls & when not to use DERMASHIELD™ 73-711
  • If chemotherapy drug compatibility is uncertain: Confirm ASTM D6978 permeation data for the exact drug, concentration, and handling conditions. Do not assume protection against every cytotoxic agent.
  • If ESD protection is required: The glove is not designated antistatic. Use an appropriately qualified ESD-protective glove system where required.
  • If sterile packaging is compromised: Do not use gloves from damaged, opened, or otherwise compromised sterile packaging.
  • If chemical resistance is critical: Verify manufacturer permeation and degradation data for the actual chemical and exposure duration.
  • If glove fit or cuff stability is inadequate: Select the appropriate size and confirm coverage with the gowning system.
  • If gloves become damaged or contaminated: Replace according to facility procedures rather than extending use beyond defined limits.
  • If expiration has passed: Do not use beyond the manufacturer's approved shelf life or labeled expiration date.

Selection rule: Sterile ISO 5 positioning, accelerator-free formulation, and ASTM D6978 chemotherapy testing do not eliminate the need for task-specific chemical compatibility assessment, operator qualification, and validated handling procedures.

Alternative sterile glove selection (when requirements change)
  • Ansell AccuTech® 91-225 Sterile Latex Gloves: A Class 100 / ISO 5 natural rubber latex option for applications where latex tactility is preferred and latex exposure is acceptable. View Product
  • Cleanroom STN1000W Series Sterile Nitrile Gloves: A 12-inch sterile nitrile glove option available in bulk-packed configurations for approved gowning and cleanroom procedures. View Product
  • Ansell BioClean™ Ultimate BUPS Sterile Neoprene Gloves: A Class 10 / ISO 4 sterile neoprene alternative for facilities with additional cleanroom cleanliness requirements. View Product

Selection principle: Evaluate sterile glove alternatives using material composition, sensitivity requirements, cleanliness performance, barrier characteristics, chemical compatibility, and gowning-system suitability.

Where DERMASHIELD™ 73-711 fits in a regulated cleanroom program
  • ISO Class 5 operations: Designed for sterile handling in critical controlled environments where documented gowning and contamination-control procedures apply.
  • EU GMP Grade A applications: Supports sterile gowning and handling programs when appropriately qualified for the facility and process.
  • Latex and accelerator exposure management: Latex-free and accelerator-free construction supports programs seeking to reduce exposure to these materials.
  • Chemotherapy-related activities: ASTM D6978 testing provides a basis for evaluating specific drug-handling applications when supported by manufacturer permeation data.
  • Intervention-heavy operations: Textured fingertips, anatomical shaping, and SUREFIT™ cuff design support controlled manipulation and stable gown interfaces.
  • Traceability programs: Sterile packaging, lot identification, and defined shelf life support receiving, inventory, and quality documentation.

Regulatory consideration: Facility-specific glove selection, gowning, disinfection, and monitoring should follow the applicable quality system. Relevant references may include ISO 14644, U.S. FDA guidance, USP <797>, USP <800>, and EU GMP Annex 1 where applicable.

Why buy Ansell DERMASHIELD™ 73-711 from SOSCleanroom
  • Authorized Ansell distributor: SOSCleanroom supports customers with Ansell sterile glove selection, product specifications, and configuration requirements.
  • Sterile configuration control: Purchasing by exact SKU, glove size, sterile packaging configuration, and case quantity helps reduce unintended substitutions.
  • Documentation support: We help customers locate manufacturer Product Data Sheets and relevant testing information for purchasing and quality-system reviews.
  • One-cart procurement: Combine sterile Ansell gloves with Texwipe sterile wipers, swabs, IPA solutions, and other cleanroom consumables used in critical environments.
Manufacturer documentation (authoritative references)
If you have any questions please email us at Sales@SOSsupply.com or give us a call at (214)340-8574. OR check out the AI ChatBot powered by SOSCleanroom data libraries - give it a try! THIS IS NEW FOR 2026! © 2026 SOSCleanroom. All rights reserved.