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RR3033

by Wright Medical Technology, Inc.

Ref RR3033Model 08897970059HNN

RR3033 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 08897970059HNN) and listed in FDA GUDID since 11 Aug 2022 (UDI-DI 00889797102742), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08897970059HNN Basic UDI-DI 00889797102742UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889797102742 UDI-DI Date11 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08897970059HNN registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 00889797102742 listed 11 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889797102742
  2. Registered EUDAMED 08897970059HNN

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Orthopaedic implant/instrument dismantling device
Device name
LE Class I Instruments - RETRACTION INSTRUMENTATION - Class I
Model / Ref / Catalog
RR3033, 08897970059HNN
Primary DI / UDI-DI
00889797102742
Basic UDI-DI
08897970059HNN
FDA product code
LXH
EMDN code
L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
GMDN term
Orthopaedic implant/instrument dismantling device
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant/instrument dismantling device

Similar devices in this category

Other devices filed under INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)