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Nuva™

by Beijing Taijieweiye Technology Co., Ltd. 152 variants

Ref TJED-D-6.5-20

Active European Union

CE MDR

Valid until

2 Jul 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 824536 Date3 Jul 2026IssuedStatusActive expires 2 Jul 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 824536 Active

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    3 Jul 2026
    Expires
    2 Jul 2031

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Nuva™ Flow Diverter
Model / Reference
TJED-D-6.5-20
Primary DI / UDI-DI
06926724006781
Basic UDI-DI
69267240TJ0029J4
EMDN Code
C010402020399 Embolisation devices - other
Device Class
Class III
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000004540
Authorised representative
Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551

Other devices from Beijing Taijieweiye Technology Co., Ltd.

See all devices from Beijing Taijieweiye Technology Co., Ltd. →

Properties

  • Sterile
  • Implantable

Other properties (11)

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