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Devon 31155297

by Cardinal Health 200, LLC

Devon 31155297 is a Class I device made by Cardinal Health 200, LLC, listed in FDA GUDID since 4 Jun 2024 (UDI-DI 50192253052655), 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 Number50192253052655 UDI-DI Date4 Jun 2024ListedStatusListed 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  • Withdrawn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
Devon
Generic name
Suturing needle holder, single-use
Model / Ref / Catalog
31155297
Primary DI / UDI-DI
50192253052655
FDA product code
GAB
GMDN term
Suturing needle holder, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

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)