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Conmed CD070

by Conmed Corporation

Part of a family of 6 devices: see the family page

Ref CD070

Conmed CD070 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 Jan 2026 (Basic UDI-DI 084585465002DM) and listed in FDA GUDID since 31 Mar 2021 (UDI-DI 20845854649616), 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 Number084585465002DM Basic UDI-DI 20845854649616UDI-DIDate30 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20845854649616 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585465002DM registered 30 Jan 2026 Active
  • FDA GUDID UDI-DI 20845854649616 listed 31 Mar 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 20845854649616
  2. Registered EUDAMED 084585465002DM

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  • Withdrawn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
Bone-resection orthopaedic reamer, reusable
Device name
Orthopedic, Non-active, Reamer, Reusable, Constant Diameter
Model / Ref / Catalog
CD070
Primary DI / UDI-DI
20845854649616
Basic UDI-DI
084585465002DM
Direct marketing DI
10845854649619
FDA product code
GFG
EMDN code
L0318 Instruments for support of surgical devices, reusable
GMDN term
Bone-resection orthopaedic reamer, reusable
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

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: Bone-resection orthopaedic reamer, reusable

Similar devices in this category

Other devices filed under INSTRUMENTS FOR SUPPORT OF SURGICAL DEVICES, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)