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Condor 48UM40A

by Grainger International, Inc.

Condor 48UM40A is a Class I device made by Grainger International, Inc., listed in FDA GUDID since 8 Oct 2025 (UDI-DI 10194484321861), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10194484321861 UDI-DI Date8 Oct 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Condor
Generic name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
48UM40A
Primary DI / UDI-DI
10194484321861
FDA product code
LZA
GMDN term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Other devices from Grainger International, Inc.

See all devices from Grainger International, Inc. →

Properties

  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)