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Carnegie Surgical LLC 304-080

by Carnegie Surgical LLC

Carnegie Surgical LLC 304-080 is a Class I device made by Carnegie Surgical LLC, listed in FDA GUDID since 8 Apr 2023 (UDI-DI G1413040800), 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 NumberG1413040800 UDI-DI Date8 Apr 2023ListedStatusListed GUDID: 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  • Withdrawn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
Carnegie Surgical LLC
Generic name
Airway tube forceps, single-use
Model / Ref / Catalog
304-080
Primary DI / UDI-DI
G1413040800
FDA product code
HTD
GMDN term
Airway tube forceps, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Airway tube forceps, single-use

Similar devices

Other devices filed under FDA product code HTD (Forceps).

Other devices from Carnegie Surgical LLC

See all devices from Carnegie Surgical LLC →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)