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Sterile PTCA Balloon Catheter

by Zhejiang Barty Medical Technology Co., Ltd. 109 variants

Ref PG40022

Active European Union

CE MDR

Valid until

14 May 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier UDEM Adriatic d.o.o.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberM.2025.MDR.2018 Date22 Jun 2026IssuedStatusActive expires 14 May 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • M.2025.MDR.2018 Active Amended

    Technical documentation EU MDR

    Certifier
    UDEM Adriatic d.o.o. 2696
    Issued
    22 Jun 2026
    Expires
    14 May 2028
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
PG40022
Primary DI / UDI-DI
06927741079390
Basic UDI-DI
69277410ZBT0001TB
EMDN Code
C010401020101 Ptca balloon dilation catheters
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000007977
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Zhejiang Barty Medical Technology Co., Ltd.

See all devices from Zhejiang Barty Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • 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