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Conmed 7-796-19BX

by Conmed Corporation

Ref 7-796-19BX

Conmed 7-796-19BX is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 26 Apr 2026 (Basic UDI-DI B-10653405004660) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10653405004660), 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-10653405004660 Basic UDI-DI 10653405004660UDI-DIDate26 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405004660 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10653405004660 registered 26 Apr 2026 Active
  • FDA GUDID UDI-DI 10653405004660 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10653405004660
  2. Registered EUDAMED B-10653405004660

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  • Withdrawn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
Medical equipment/instrument drape, single-use
Device name
Non-orthopedic, Non-active, Accessory, Drape/Sheath/Cover, Handpiece, Sterile
Model / Ref / Catalog
7-796-19BX
Primary DI / UDI-DI
10653405004660
Basic UDI-DI
B-10653405004660
FDA product code
GEI
EMDN code
T030199 Covers, instruments and equipment - other
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4400
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 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: Medical equipment/instrument drape, single-use

Similar devices in this category

Other devices filed under COVERS, INSTRUMENTS AND EQUIPMENT - OTHER.

Other devices from Conmed Corporation

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Properties

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