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MediChoice GZBN1003

by Owens & Minor Distribution, Inc.

MediChoice GZBN1003 is a Class I device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 16 Sep 2020 (UDI-DI 10885632069789), 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 Number10885632069789 UDI-DI Date16 Sep 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  • Withdrawn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
Woven gauze roll/sheet
Model / reference
GZBN1003
Primary DI / UDI-DI
10885632069789
FDA product code
NAB
GMDN term
Woven gauze roll/sheet
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Related devices

Category: Woven gauze roll/sheet

Similar devices

Other devices filed under FDA product code NAB (Gauze / sponge,nonresorbable for external use).

Other devices from Owens & Minor Distribution, Inc.

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

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)