Skip to content

MediChoice GLV1003

by Owens & Minor Distribution, Inc.

MediChoice GLV1003 is a Class I device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 5 Oct 2020 (UDI-DI 30885632110966), 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 Number30885632110966 UDI-DI Date5 Oct 2020ListedStatusListed 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  • Withdrawn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
MediChoice
Generic name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
GLV1003
Primary DI / UDI-DI
30885632110966
FDA product code
LYY
GMDN term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LYY (Latex patient examination glove).

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)