Where XC-310 fits (and where it does not)
XC-310 is typically chosen for labs, staging, and controlled support zones where teams want reliable barrier performance and confident dexterity without the bulk of heavier disposable gloves. It is a practical option for sampling, inspection, routine handling, and "high-touch" workflows that require frequent glove changes. It is also non-sterile, so if your SOP requires sterile cleanroom gloves in ISO Class 4–5 environments or EU GMP Grade A/B operations, treat that as a separate glove category selection.
What the manufacturer publishes (short version)
- Material: nitrile; powder-free; not made from natural rubber latex.
- Grip: textured fingers for tool and component handling.
- Barrier integrity: 0.65 AQL (freedom from holes, Inspection Level I).
- Thin profile for feel: typical palm 0.07 mm; finger 0.11 mm.
- Format: 250 gloves per dispenser; 10 dispensers per case (XL packaging differs).
Donning education (ISO first, then Annex 1)
ISO cleanroom programs emphasize operational control. ISO 14644-5 describes an operations control program that includes personnel management and a gowning program. Gloves are not an isolated purchase — they are part of your contamination-control system.
Clean donning habits that reduce contamination transfer
- Begin clean and dry: wash and dry hands fully before donning.
- Touch the minimum: contact only the inside of the cuff while donning.
- No cuff "snap": can generate particles and encourages glove damage.
- Change often, by rule: define glove-change triggers and enforce them.
- Use a two-layer approach when appropriate: underglove for stability + outer glove changed more frequently.
EU GMP Annex 1 context: sterile manufacturing programs require disciplined glove use including disinfection and defined replacement intervals in Grade A/B areas. Annex 1 thinking pushes teams toward fewer touchpoints, clearer procedures, and fewer undocumented exceptions.
Specifications in context
| Attribute |
XC-310 (published) |
| Material / format | Nitrile; powder-free; textured fingers |
| Barrier integrity | 0.65 AQL (freedom from holes, Inspection Level I) |
| Thickness (typical) | Palm 0.07 mm / Finger 0.11 mm |
| Length (typical) | 240 mm (9.5 in) |
| Antistatic | Yes |
| Packaging | 250/dispenser; 10 dispensers/case (XL differs) |
| Sterility | Non-sterile |
Standards and documentation
Manufacturers publish standards and regulatory statements to help customers align glove selection with application risk and medical exam expectations. Your internal SOP still governs what is acceptable for your process. For high-scrutiny environments, keep the glove PDS/CoC with the receiving record so audits do not become a scramble.
SOSCleanroom + Ansell (including KleenGuard)
Customers increasingly want to standardize PPE across glove, garment, and eye/face protection. As Ansell's portfolio expands to include brands such as KleenGuard and Kimtech in key markets, SOSCleanroom is building cleaner product families so teams can reduce supplier fragmentation, simplify approvals, and keep programs consistent across sites.
Common failure modes
- "I wore the same gloves everywhere" drift: define change triggers and enforce them.
- Overhandling during donning: train to contact only the inside cuff and stop readjusting.
- False cleanroom assumptions: non-sterile exam gloves are not automatically acceptable in aseptic cores — match glove category to SOP.
- Packaging misuse: keep dispensers protected and away from splash/overspray zones.
SOSCleanroom note about SOPs
The Technical Vault is written to help customers strengthen contamination-control thinking. It is not your facility SOP, validation protocol, or regulatory determination.
Always verify glove suitability, documentation requirements, and acceptance criteria using your internal quality system.
Source basis
SOSCleanroom is the source for this Technical Vault entry.
Briefed and approved by the SOSCleanroom (SOS) staff.
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Last reviewed: May 1, 2026
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