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Convertors 2111PG

by Cardinal Health 200, LLC

Convertors 2111PG is a Class I device made by Cardinal Health 200, LLC, listed in FDA GUDID since 5 Jun 2019 (UDI-DI 20885380041058), 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 Number20885380041058 UDI-DI Date5 Jun 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  • Withdrawn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
Convertors
Generic name
Isolation gown, single-use
Model / Ref / Catalog
2111PG
Primary DI / UDI-DI
20885380041058
FDA product code
OEA
GMDN term
Isolation gown, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Isolation gown, single-use

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)