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Hip Instruments 20.00002

by Medacta International SA

Hip Instruments 20.00002 is a Class I device made by Medacta International SA, listed in FDA GUDID since 29 Jul 2022 (UDI-DI 07630345717849), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07630345717849 UDI-DI Date29 Jul 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  • Withdrawn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
Hip Instruments
Generic name
Orthopaedic cement injection cannula
Model / reference
20.00002
Description
AMIS Nozzle - Instrument set EASYMIX
Primary DI / UDI-DI
07630345717849
FDA product code
GEA
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

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Other devices filed under Orthopaedic cement injection cannula.

Other devices from Medacta International SA

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Properties

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