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Revision Cannula ASA0050

by Tecres

Revision Cannula ASA0050 is a Class I device made by Tecres, listed in FDA GUDID since 23 Sep 2022 (UDI-DI 08031497002224), 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 Number08031497002224 UDI-DI Date23 Sep 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  • Withdrawn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
Revision Cannula
Generic name
Orthopaedic cement injection cannula
Model / reference
ASA0050
Primary DI / UDI-DI
08031497002224
FDA product code
KDD
GMDN term
Orthopaedic cement injection cannula
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic cement injection cannula

Similar devices in this category

Other devices filed under Orthopaedic cement injection cannula.

Other devices from Tecres

See all devices from Tecres →

Properties

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