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VitaFlow LibertyTM Delivery System, Loading Tool, Battery

by Shanghai MicroPort CardioFlow Medtech Co., Ltd. 4 variants

Ref DSR21, LT-21, BAT1200

Active European Union

CE MDR

Valid until

1 Apr 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier DEKRA Certification B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6126688CE01 Date15 Oct 2025IssuedStatusActive expires 1 Apr 2029

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 6126688CE01 Active Amended

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    15 Oct 2025
    Expires
    1 Apr 2029
    Reason
    Mnf data change
  • 6126688TD01 Active Amended

    Technical documentation EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    15 Oct 2025
    Expires
    1 Apr 2029
    Reason
    Mnf data change

Coverage

1 jurisdiction

DenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumCzech RepublicSlovakiaAustriaHungaryRomaniaPortugalSpainItalyGreece
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 17 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria
  • Belgium
  • Czechia
  • Denmark since 24 Apr 2024
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain

Last checked 30 Oct 2026.

Specification

EUDAMED

Device Name
VitaFlow LibertyTM Transcatheter Aortic Valve System
Model / Reference
DSR21, LT-21, BAT1200
Primary DI / UDI-DI
06971493530630
Basic UDI-DI
697149353Z0213CEEU
EMDN Code
P07038002 Cardiac valve transcatheter implant accessories
Device Class
Class III
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
CN-MF-000002327
Authorised representative
MicroPort Medical B.V. NL-AR-000000166

Other devices from Shanghai MicroPort CardioFlow Medtech Co., Ltd.

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Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No