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Conmed PRO1232PD

by Conmed Corporation

Ref PRO1232PD

Conmed PRO1232PD is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 30 Jul 2026 (Basic UDI-DI 084585408765E3) and listed in FDA GUDID since 9 Jun 2023 (UDI-DI 10845854083710), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408765E3 Basic UDI-DI 10845854083710UDI-DIDate30 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854083710 UDI-DI Date9 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408765E3 registered 30 Jul 2026 Active
  • FDA GUDID UDI-DI 10845854083710 listed 9 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854083710
  2. Registered EUDAMED 084585408765E3

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  • Withdrawn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

Trade name
Conmed
Generic name
Pin-driving power tool attachment
Device name
Orthopedic, Active, Attachment, Pin Driver, All
Model / Ref / Catalog
PRO1232PD
Primary DI / UDI-DI
10845854083710
Basic UDI-DI
084585408765E3
Direct marketing DI
20845854083717
FDA product code
HWE
EMDN code
Z12130599 Motorised orthopaedic surgery system instruments - other
GMDN term
Pin-driving power tool attachment
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Pin-driving power tool attachment

Similar devices in this category

Other devices filed under MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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