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Magnet TAC004C

by Microport Crm SRL

Ref TAC004CModel Magnet

Magnet TAC004C is a Class I device made by Microport Crm SRL, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI 8031527MAGNET0000000001ZG) and listed in FDA GUDID since 23 Sep 2021 (UDI-DI 08031527019956), active as of 7 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number8031527MAGNET0000000001ZG Basic UDI-DI 08031527019956UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08031527019956 UDI-DI Date23 Sep 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 8031527MAGNET0000000001ZG registered 6 Nov 2026 Active
  • FDA GUDID UDI-DI 08031527019956 listed 23 Sep 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08031527019956
  2. Registered EUDAMED 8031527MAGNET0000000001ZG

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  • Withdrawn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
Magnet
Generic name
Cardiac pulse generator test magnet
Model / Ref / Catalog
TAC004C, Magnet
Primary DI / UDI-DI
08031527019956
Basic UDI-DI
8031527MAGNET0000000001ZG
FDA product code
DTG
EMDN code
J019003 Active-implantable cardiac systems magnetised devices
GMDN term
Cardiac pulse generator test magnet
Device class
Class I
Regulation number
870.3690
EU registration type
Standard device
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution

Other devices from Microport Crm SRL

See all devices from Microport Crm SRL →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (22, all answered No)