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Vitegra® JESTTH

by Joimax GmbH

Ref JESTTH

Vitegra® JESTTH is a Class I device made by Joimax GmbH, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 42503371VIDOAG7) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337119821), active as of 12 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503371VIDOAG7 Basic UDI-DI 04250337119821UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337119821 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371VIDOAG7 registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04250337119821 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337119821
  2. Registered EUDAMED 42503371VIDOAG7

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  • Withdrawn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
Halteadapter EUDAMED
Vitegra® GUDID
Generic name
Medical image management system
Model / Ref / Catalog
JESTTH
Primary DI / UDI-DI
04250337119821
Basic UDI-DI
42503371VIDOAG7
FDA product code
LMB
EMDN code
Z12020480 Instruments for the acquisition and management of endoscopic and minimally invasive surgery images - hardware accessories
GMDN term
Medical image management system
Device class
Class I
Regulation number
892.2010
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical image management system

Similar devices in this category

Other devices filed under INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES.

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)