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Conmed 001429

by Conmed Corporation

Ref 001429

Conmed 001429 is an endoscopic bite block (EU MDR Class I; FDA Class II; FDA product code KTI, Bronchoscope Accessory) made by Conmed Corporation, registered in EUDAMED on 27 Oct 2025 (Basic UDI-DI 084585408511D2) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 20653405053887), 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 Number084585408511D2 Basic UDI-DI 20653405053887UDI-DIDate27 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number20653405053887 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408511D2 registered 27 Oct 2025 Active
  • FDA GUDID UDI-DI 20653405053887 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 20653405053887
  2. Registered EUDAMED 084585408511D2

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  • Withdrawn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
Endoscopic bite block, basic, single-use
Device name
Non-orthopedic, Non-active, Accessory, Bite Block
Model / Ref / Catalog
001429
Primary DI / UDI-DI
20653405053887
Basic UDI-DI
084585408511D2
Unit of use DI
00653405053883
FDA product code
KTI
EMDN code
G030804 Gastrointestinal endoscopy and echoendoscopy, bite blocks
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
874.4680
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Length — 27 Millimeter
Width — 20 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under GASTROINTESTINAL ENDOSCOPY AND ECHOENDOSCOPY, BITE BLOCKS.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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