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Conmed 129

by Conmed Corporation

Ref 129

Conmed 129 is a device classified as Class IIa in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI B-10653405052371) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10653405052371), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10653405052371 Basic UDI-DI 10653405052371UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405052371 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10653405052371 registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 10653405052371 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10653405052371
  2. Registered EUDAMED B-10653405052371

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  • Withdrawn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
Flexible endoscopic cytology brush, single-use
Device name
Endoscopic Surgical Instruments
Model / Ref / Catalog
129
Primary DI / UDI-DI
10653405052371
Basic UDI-DI
B-10653405052371
FDA product code
FDX
EMDN code
Z12029099 Various instruments for endoscopy and mini–invasive surgery – other
GMDN term
Flexible endoscopic cytology brush, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Outer Diameter — 2 Millimeter
Length — 11 Millimeter
Length — 120 Millimeter
Outer Diameter — 1.7 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 10653405052371: EUDAMED states No, FDA GUDID states Yes.

Device class is stated on each registry's own scale: Class IIa 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: Flexible endoscopic cytology brush, single-use

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI–INVASIVE SURGERY – OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)