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Conmed C6176

by Conmed Corporation

Ref C6176

Conmed C6176 is a bone-coring punch (EU MDD Class I; FDA Class I; FDA product code NBH, Accessories,Arthroscopic) made by Conmed Corporation, registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-10845854031018) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854031018), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854031018 Basic UDI-DI 10845854031018UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854031018 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854031018 registered 26 May 2026 Active
  • FDA GUDID UDI-DI 10845854031018 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854031018
  2. Registered EUDAMED B-10845854031018

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  • Withdrawn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-coring punch, reusable
Device name
Reusable Manual Surgical Instruments
Model / Ref / Catalog
C6176
Primary DI / UDI-DI
10845854031018
Basic UDI-DI
B-10845854031018
FDA product code
NBH
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Bone-coring punch, reusable
Device class
Class I
Regulation number
888.1100
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 2.1 Millimeter

Related devices

Category: Bone-coring punch, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (18, all answered No)