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Conmed Linvatec N-Perc

by Conmed Corporation

Ref N-PERC

Conmed Linvatec N-Perc is an arthroscopic surgical procedure kit (EU MDD Class IIa; FDA Class I; FDA product code KDD, Kit, surgical instrument, disposable) made by Conmed Corporation, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI B-10845854036594) and listed in FDA GUDID since 5 May 2022 (UDI-DI 10845854036594), 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-10845854036594 Basic UDI-DI 10845854036594UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854036594 UDI-DI Date5 May 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854036594 registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 10845854036594 listed 5 May 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854036594
  2. Registered EUDAMED B-10845854036594

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  • Withdrawn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 Linvatec
Generic name
Arthroscopic surgical procedure kit, non-medicated, single-use
Device name
Disposable Surgical Instruments
Model / Ref / Catalog
N-PERC
Primary DI / UDI-DI
10845854036594
Basic UDI-DI
B-10845854036594
FDA product code
KDD
EMDN code
T0202 Surgical procedural kits (excluding surgical instrument kits)
GMDN term
Arthroscopic surgical procedure kit, non-medicated, single-use
Device class
Class IIa EUDAMED
Class I GUDID
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
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: Arthroscopic surgical procedure kit, non-medicated, single-use

Similar devices in this category

Other devices filed under PROTECTIVE CLOTHING AND DRAPES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE).

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)