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Convertors 8145W

by Cardinal Health 200, LLC

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885380034339 UDI-DI Date9 May 2018ListedStatusListed GUDID: not 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  • Withdrawn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
Convertors
Generic Name
Patient surgical drape, single-use, non-sterile
Model / Ref / Catalog
8145W
Primary DI / UDI-DI
00885380034339
FDA Product Code
PUI
GMDN Term
Patient surgical drape, single-use, non-sterile
Device Class
Class II
Regulation Number
878.4370
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Ethylene Oxide

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Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No