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Cardinal Health G4BB

by Cardinal Health 200, LLC

Cardinal Health G4BB is a Class I device made by Cardinal Health 200, LLC, listed in FDA GUDID since 10 Apr 2019 (UDI-DI 10885380070419), 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 Number10885380070419 UDI-DI Date10 Apr 2019ListedStatusListed 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  • Withdrawn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
Cardinal Health
Generic name
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
G4BB
Primary DI / UDI-DI
10885380070419
FDA product code
MNK
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under Endoscopic bite block, basic, single-use.

Other devices from Cardinal Health 200, LLC

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)