Ansell Brochures

Document-to-product workflow

Start with the hazard assessment, not the brand name.

A catalogue is the beginning of a selection process, not the final qualification record. Ansell supplies products for very different tasks: sterile aseptic work, clean but nonsterile microelectronics handling, hazardous-chemical splash, fixed isolator ports and industrial maintenance. These applications do not share one interchangeable glove or garment specification.

Use this page as a document-and-product crosswalk. Start with a manufacturer brochure to identify a family; move to the exact style-number technical data sheet to validate construction and intended use; obtain product- or batch-specific certificates where applicable; then complete the facility-specific risk assessment, operator fit trial and change-control approval.

Manufacturer library

Ansell catalogues, brochure PDFs and the live resource center.

The following resource links are hosted by Ansell unless otherwise noted. Large manufacturer catalogues can be tens of megabytes and may load slowly or be blocked by some browsers. Ansell can revise or retire a PDF without notice; if a link is inaccessible, use the live BioClean resource hub or Ansell Resources Center to locate the latest issue.

Read documentation correctly

Catalogue, technical data sheet, certificate and permeation report are different evidence.

For controlled purchasing, store a document title, revision or issue date, publisher, downloaded filename, exact model identifier and retrieval date in your master approved-product file. When the manufacturer updates a data sheet, assess the change instead of silently overwriting the qualification evidence.

Application matrix

Choose PPE according to the environment and hazard profile.

Cleanroom gloving

Nonsterile cleanroom processing and sterile packaging answer different questions.

Ansell cleanroom gloves include both nonsterile cleanroom-processed gloves and sterile gloves. Buyers should evaluate the process-relevant data instead of assuming every nitrile glove has comparable residue control, sterile presentation or chemical protection.

For the documented differences between 93-401 and sterile models, refer to the manufacturer Nitrilite 93-401 data sheet, BioClean Excell BEXS data sheet and TouchNTuff 93-700 data sheet.

Sterile glove programs

Translate sterile-product documents into gowning and aseptic technique.

For aseptic processing and sterile compounding, a sterile glove must remain appropriately protected until use, be donned according to the site procedure and remain suitable through the actual manipulations. Evaluate how gloves work with gown sleeves, sterile disinfectants, equipment interfaces and repeated movements.

Permeation and chemical hazards

A product brochure cannot replace chemical or chemotherapy-drug compatibility testing.

A chemical-resistant claim describes performance under specified test conditions, not unlimited exposure. Distinguish permeation (molecular transport through intact material), penetration (movement through defects) and degradation (physical or chemical material change).

For ordinary chemical splash tasks, Ansell TouchNTuff 92-600 is a nonsterile nitrile candidate; SOSCleanroom specifically lists it as not chemotherapy-drug tested. For sterile handling where chemotherapy testing is relevant, evaluate Ansell TouchNTuff 93-700 or Ansell BioClean Emerald BENS only after reviewing the actual drug-specific permeation documentation.

Ansell offers AnsellGUARDIAN chemical selection resources through its manufacturer site. Use the product model, actual chemical, concentration, temperature, contact duration and operation to interpret available results.

Barrier equipment interfaces

RABS and isolator glove selection must begin with the installed hardware.

Restricted Access Barrier Systems (RABS) and isolators commonly use fixed glove assemblies as part of their containment boundary. A conventional disposable glove cannot substitute for a machine-specific gloveport assembly. Select according to port diameter, attachment method, glove length, polymer, resistance to the decontamination cycle, sterility, integrity testing and installation procedure.

Gowning and contamination control

Evaluate garments, gloves and head protection as one system.

Cleanroom garments are a contamination-control system, not simply clothing. Body coverage, garment material, seaming, zipper/placket construction, cuff retention, sterile fold, packaging, and movement-related shedding should all be considered. A sterile label does not eliminate the need for controlled gowning technique.

Link garment selection to documented procedures, including gowning order, glove-to-sleeve interfaces, garment change triggers, approved disinfection and movement restrictions. For context see SOSCleanroom reusable versus disposable garments and the USP glove selection guide.

Face and eye protection

Goggles are a product-protection and worker-protection decision.

Eye and face protection should be chosen by the actual exposure hazard, splash risk, cleanroom requirements, visibility and reprocessing capabilities. Sterile disposable goggles and reusable autoclavable goggles are not the same purchasing or qualification decision.

Verify compatibility with the facility mask, hood, corrective eyewear and use of disinfectants. Consider anti-fog properties and indirect ventilation, but use manufacturer documents and the hazard assessment to determine suitability. The decision to reuse must include reliable tracking of cleaned, processed and released items.

Electronics and microelectronics

Match antistatic protection and cleanroom cleanliness separately.

Microelectronics, semiconductor and photolithography processes may be sensitive to particles, extractable ions, electrostatic discharge (ESD), molecular contaminants and direct physical contact. Ansell's 2022 microelectronics selection flyer explicitly treats cleanliness, sterility, antistatic behavior, gowning, material, sizing and chemical protection as separate procurement criteria.

Product families and boundaries

An industrial safety glove is not automatically a critical cleanroom glove.

Ansell's larger portfolio includes industrial handling gloves such as HyFlex, chemical-splash products such as TouchNTuff, and specialized cleanroom PPE under BioClean/Nitrilite. Only products supplied and documented for the required contamination-controlled environment should be considered for exposed-product critical activities.

Interpret compliance claims

What published standards can and cannot prove.

Published standards and manufacturer documentation can be amended. Always verify the current test edition, regional declaration, exact style and revision before final approval. Older brochures may contain historical test notations that differ from current manufacturer data sheets.

Batch documentation

Make certificates, technical data and received lots traceable.

A certificate search is particularly useful when the receiving team needs evidence tied to an actual lot. Ansell's official Certificate Search supports certificate retrieval for eligible clean and sterile styles, including CoA/CoC/CoI categories. The required identifier can differ by family.

Material transfer discipline

The package is part of the contamination-control system.

For critical areas, the outside shipping carton should not be confused with a cleanroom-compatible inner bag or sterile barrier. Multiple nested packaging layers allow controlled transfers, but the facility must still determine when each layer is removed and how contamination is prevented.

For a detailed documented example, see BEXS product data and 93-700 product data, which describe sterile glove configurations and packaging considerations. Actual package quantities and variants should always be checked at the point of order.

Ergonomic qualification

Sizing, cuff length and dexterity belong in the purchase specification.

Incorrect sizing can increase strain, tearing, cuff roll-down, fingertip folds, loss of grip and discomfort. Use the manufacturer-specific chart and a documented operator trial; nominal sizes are not necessarily interchangeable across models or between sterile and nonsterile product families.

Use the SOSCleanroom Glove Sizing Chart and document an approved size matrix by operator and glove model.

Direct SOSCleanroom shopping

Sixteen Ansell product links organized by documented application.

Each link below leads to a specific SOSCleanroom listing, not a generic manufacturer search page. These are catalogue examples for technical evaluation, not statements of regulatory approval for a particular facility or drug. Confirm the current model options, size, case quantity and manufacturer documents when ordering.

Browse the wider Ansell collection, Ansell sterile nitrile gloves, Ansell apparel and Ansell isolator glove category when a current catalog variation or alternate style must be investigated.

Approval and purchasing control

A repeatable eight-step process for qualifying Ansell PPE.

Continuity of supply

Prevent undocumented PPE substitutions across shifts and sites.

Shortages or price pressure can introduce inappropriate substitutions. Two nitrile gloves may differ in polymer formulation, surface treatment, additives, cleanroom processing, sterility, packaging, particle results, cuff design and chemical breakthrough. Replacing one with the other without technical review can invalidate operator training or a facility acceptance basis.

Even a manufacturer-recommended alternative is a candidate until the facility has reviewed and approved the specific change. If the model is discontinued, use a structured model-to-model comparison rather than a general material-family substitution.

Practical examples

How different Ansell documents lead to different PPE decisions.

Frequently asked questions

Answers for cleanroom users, QA and procurement teams.

Continue your learning

Connect Ansell documents with the SOSCleanroom knowledge base.

Official manufacturer references

Document the source and its limitations before you rely on a claim.

Publication and access note: Ansell's large life-sciences and isolator PDFs are linked from its current BioClean resource hub but could not be fully retrieved by the verification tool due to file-size/access limits. The 2018 archive and 2022 microelectronics flyer were inspected directly. Always check the manufacturer for a newer issue and validate product-level documentation before release.

SOSCLEANROOM  |  ANSELL PPE STANDARDIZATION & B2B SOURCING

Bring Your Ansell Specifications, Sizes and Documentation Into One Program.

Tell us what you use, where you use it, which chemicals or hazards are present, and how your team needs to receive it. SOSCleanroom can help build a product shortlist, source requested Ansell documentation, review available SKUs and discuss recurring purchasing—while your quality and EHS teams retain approval authority.

Questions? 800-443-7101  |  sales@sossupply.com