How to Specify an Isolator Glove: Port, Material, Thickness and Sterilization

A practical inquiry checklist covering process media, material, port diameter, thickness, length, hand configuration and documentation.

How to Specify an Isolator Glove: Port, Material, Thickness and Sterilization
Technical guide

A practical inquiry checklist covering process media, material, port diameter, thickness, length, hand configuration and documentation.

Quick answer

A useful isolator glove inquiry should state the application, contact media and concentration, sterilization cycle, port diameter, required thickness and length, hand configuration, color, quantity and documentation needs.

1. Define the application and exposure

Begin with the process because it drives every later decision. State whether the glove is used in an aseptic isolator, containment system, chemical enclosure, nuclear glovebox or controlled-atmosphere manufacturing equipment.

  • All contact media and concentrations
  • Contact duration and frequency
  • Operating and cleaning temperatures
  • Required gas or vapor barrier performance

2. Describe the sterilization cycle

State VHP, steam/autoclave, gamma, ozone or another route, together with temperature, dose or concentration, exposure time and expected cycle count. This information is necessary to compare EPDM, CSM and Butyl accurately.

3. Confirm port and glove dimensions

Item What to provide Port diameter 7, 8, 9 or 10 in Thickness 15, 24, 30 or 39 mil, depending on material Length Required overall length and equipment clearance Hand configuration Ambidextrous or dedicated left/right configuration Cuff / bead interface Port drawing or existing glove reference

4. List documentation and delivery needs

  • Required test report, certificate or batch documentation
  • Packing, labeling and traceability requirements
  • Sample quantity and target production quantity
  • Required delivery date and destination country

Copy-and-send inquiry checklist

Application: __________

Contact media / concentration: __________

Sterilization cycle: __________

Material preference: EPDM / CSM / Butyl / Need recommendation

Port / thickness / length: __________

Quantity and documents: __________

Send the completed information to lee.cheng@kingsurebiotech.com.

Technical information is provided as a selection reference. Final suitability must be confirmed using the actual equipment, media, sterilization cycle and validation requirements.