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Convertors 29444N

by Cardinal Health 200, LLC 2 variants

Convertors 29444N is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 17 Nov 2017 (UDI-DI 50885380141049), 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 Number50885380141049 UDI-DI Date17 Nov 2017ListedStatusListed 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  • Withdrawn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
Convertors
Generic name
Patient surgical drape, single-use
Model / Ref / Catalog
29444N
Primary DI / UDI-DI
50885380141049
FDA product code
PUI
GMDN term
Patient surgical drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Patient surgical drape, single-use

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Sterilise before use
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)