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Conmed C8536.1

by Conmed Corporation

Ref C8536.1

Conmed C8536.1 is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854034217) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854034217), 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-10845854034217 Basic UDI-DI 10845854034217UDI-DIDate29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854034217 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854034217 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854034217 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854034217
  2. Registered EUDAMED B-10845854034217

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  • Withdrawn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 file/rasp, manual, reusable
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
Model / Ref / Catalog
C8536.1
Primary DI / UDI-DI
10845854034217
Basic UDI-DI
B-10845854034217
FDA product code
NBH
EMDN code
L03130401 Tissue and organ grasping forceps, reusable
GMDN term
Bone file/rasp, manual, 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
Angle — 90 degree

Related devices

Category: Bone file/rasp, manual, reusable

Similar devices in this category

Other devices filed under TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE.

Other devices from Conmed Corporation

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Properties

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