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Centurion I67985

by Centurion Medical Products 3 variants

Centurion I67985 is a Class I device made by Centurion Medical Products, listed in FDA GUDID since 1 Jan 2022 (UDI-DI 00653160226119), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00653160226119 UDI-DI Date1 Jan 2022ListedStatusListed 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  • Withdrawn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
Centurion
Generic name
Airway tube forceps, single-use
Model / Ref / Catalog
I67985
Primary DI / UDI-DI
00653160226119
FDA product code
BWB
GMDN term
Airway tube forceps, single-use
Device class
Class I
Regulation number
868.5780
GUDID distribution status
In Commercial Distribution

Related devices

Category: Airway tube forceps, single-use

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)