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Conmed 8212

by Conmed Corporation

Ref 8212

Conmed 8212 is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854029985) and listed in FDA GUDID since 6 Oct 2021 (UDI-DI 10845854029985), active as of 23 Oct 2026.

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

CE MDD

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854029985 Basic UDI-DI 10845854029985UDI-DIDate29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854029985 UDI-DI Date6 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854029985 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854029985 listed 6 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854029985
  2. Registered EUDAMED B-10845854029985

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Bone curette, reusable
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Scraping
Model / Ref / Catalog
8212
Primary DI / UDI-DI
10845854029985
Basic UDI-DI
B-10845854029985
FDA product code
MDM
EMDN code
L0901 Orthopaedic surgery spoons and curettes, reusable
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 10845854029985: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Bone curette, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use YesEUDAMEDNoGUDID
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)