Skip to content

Posi-Prene Green 2400PF/XL

by Clinical Supply

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850006162642 UDI-DI Date24 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Posi-Prene Green
Generic Name
Polychloroprene examination/treatment glove, non-powdered
Model / Reference
2400PF/XL
Primary DI / UDI-DI
00850006162642
FDA Product Code
LZA
GMDN Term
Polychloroprene examination/treatment glove, non-powdered
Device Class
Class I
Regulation Number
880.6250
GUDID distribution status
In Commercial Distribution

Other devices from Clinical Supply

See all devices from Clinical Supply →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No