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MicroPort CRM S.r.l.

Italy Last updated 25 Oct 2026

Devices
79
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue79

Page 2 of 2

Showing 51-79 of 79

EUDAMED certificates1

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G70 005178 0044 Reissued

    Technical documentation EU MDR

    Issued
    14 Sep 2026
    Expires
    12 Dec 2031
    Valid from
    13 Dec 2026

Notified bodies

What MicroPort CRM S.r.l. makes

MicroPort CRM S.r.l. manufactures implantable cardiac devices, including implantable cardioverter-defibrillators (ICDs) branded as PLATINIUM, pacemaker systems with MRI-compatible designs (KORA), and a remote monitoring system (HookUp Smart). Their portfolio also includes specific pacemaker and defibrillator models with regional designations (e.g., V209-RC042EU/JP, RC032).

The company’s devices fall under Active Implantable Medical Device Directive (AIMDD) classifications, with most listed as Class I or Class IIa. These products are registered in the EU’s eudamed database, adhering to European regulatory requirements. The manufacturer is based in Italy.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Address
s.n., Via Crescentino, Saluggia (VC), Italy
PRRC contact
Anne ROUSSEAU-PLASSE
EUDAMED SRN
IT-MF-000029013
FDA FEI number
1000165971