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Cardinal Health PBCGGDBM7

by Cardinal Health 200, LLC

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 Number10197106316184 UDI-DI Date15 Jun 2023ListedStatusListed 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  • Withdrawn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
Cardinal Health
Generic Name
Laparoscopic surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
PBCGGDBM7
Primary DI / UDI-DI
10197106316184
FDA Product Code
OHD
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, single-use
Device Class
Class II
Regulation Number
884.1720
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laparoscopic surgical procedure kit, non-medicated, single-use

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (5)

  • Implantable: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No