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Conmed 32.10018

by Conmed Corporation

Ref 32.10018

Conmed 32.10018 is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854038048) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854038048), 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-10845854038048 Basic UDI-DI 10845854038048UDI-DIDate29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854038048 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854038048 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854038048 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854038048
  2. Registered EUDAMED B-10845854038048

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
Model / Ref / Catalog
32.10018
Primary DI / UDI-DI
10845854038048
Basic UDI-DI
B-10845854038048
FDA product code
GEN
EMDN code
L091202 Orthopaedic surgery files, reusable
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, 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
Sterilisation method
Moist Heat or Steam Sterilization
Size
Angle — 45 degree
Width — 2.75 Millimeter
Length — 130 Millimeter

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC RASPS AND FILES, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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