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Conmed 00702129200

by Conmed Corporation

Ref 7021-292

Conmed 00702129200 (7021-292) is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 17 Jul 2026 (Basic UDI-DI B-10845854005361) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854005361), 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-10845854005361 Basic UDI-DI 10845854005361UDI-DIDate17 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854005361 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854005361 registered 17 Jul 2026 Active
  • FDA GUDID UDI-DI 10845854005361 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854005361
  2. Registered EUDAMED B-10845854005361

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  • Withdrawn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
Orthopaedic bur, single-use
Device name
Orthopedic, Non-active, Handpiece Bur
Model / Ref / Catalog
7021-292, 00702129200
Primary DI / UDI-DI
10845854005361
Basic UDI-DI
B-10845854005361
FDA product code
GFF
EMDN code
K030204 Arthroscopy burs, single-use
GMDN term
Orthopaedic bur, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 25.4 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
7021-292
GUDID
00702129200
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: Orthopaedic bur, single-use

Similar devices in this category

Other devices filed under ARTHROSCOPY BURS, SINGLE-USE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)