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Conmed 000615

by Conmed Corporation

Ref 000615

Conmed 000615 is a Class I device made by Conmed Corporation, registered in EUDAMED on 11 Nov 2025 (Basic UDI-DI 084585408530D6) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10653405050315), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408530D6 Basic UDI-DI 10653405050315UDI-DIDate11 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405050315 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408530D6 registered 11 Nov 2025 Active
  • FDA GUDID UDI-DI 10653405050315 listed 24 Sep 2020 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 10653405050315
  2. Registered EUDAMED 084585408530D6

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Surgical instrument/endoscope cleaning utensil, single-use
Device name
Non-orthopedic, Non-active, Accessory, Endoscope Cleaning
Model / Ref / Catalog
000615
Primary DI / UDI-DI
10653405050315
Basic UDI-DI
084585408530D6
Unit of use DI
00653405050318
FDA product code
MNL
EMDN code
V070101 Endoscopes cleaning brushes - for generic use
GMDN term
Surgical instrument/endoscope cleaning utensil, single-use
Device class
Class I
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Length — 230 Centimeter
Outer Diameter — 2 Millimeter

Similar devices in this category

Other devices filed under CLEANING BRUSHES.

Other devices from Conmed Corporation

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)