Skip to content

MVC Pro

by MediCapture, Inc.

Ref MVC410

MVC Pro (MVC410) is a video image processor (EU MDR Class I; FDA Class I; FDA product code LMD, System, Digital Image Communications, Radiological) made by Medicapture, Inc., registered in EUDAMED on 8 Jan 2025 (Basic UDI-DI 0859151005MVC410ZP) and listed in FDA GUDID since 12 Feb 2020 (UDI-DI 00859151005156), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0859151005MVC410ZP Basic UDI-DI 00859151005156UDI-DIDate8 Jan 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00859151005156 UDI-DI Date12 Feb 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0859151005MVC410ZP registered 8 Jan 2025 Active
  • FDA GUDID UDI-DI 00859151005156 listed 12 Feb 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00859151005156
  2. Registered EUDAMED 0859151005MVC410ZP

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  • Withdrawn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
MVC Pro EUDAMED
Mvc GUDID
Generic name
Video image processor
Device name
Video Converter
Model / reference
MVC410
Primary DI / UDI-DI
00859151005156
Basic UDI-DI
0859151005MVC410ZP
FDA product code
LMD
EMDN code
Z119080 Various bioimaging and radiotherapy instruments - hardware accessories
GMDN term
Video image processor
Device class
Class I
Regulation number
892.2020
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
US-MF-000013680
Authorised representative
MEDICAPTURE EUROPE B.V. NL-AR-000018862

Similar devices in this category

Other devices filed under VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Medicapture, Inc.

  • MTR245W

    Class I

  • MTS156W

    Class I

  • MTR133W

    Class I

  • MSP245

    Class I

See all devices from Medicapture, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)