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Disposable Biopsy Valve

by Zhuji Pengtian Medical Instrument Co., Ltd 3 variants

Ref PT-HJF-02Model PT-HJF-01

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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 Number69501904biopsyvalveL6 Basic UDI-DI 06950190422226UDI-DIDate12 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Disposable Biopsy Valve
Model / Reference
PT-HJF-01, PT-HJF-02
Primary DI / UDI-DI
06950190422226
Basic UDI-DI
69501904biopsyvalveL6
EMDN Code
Z12029085 Various instruments for endoscopy and mini-invasive surgery - consumables
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
CN-MF-000013084
Authorised representative
Meditech X-Ray Spółka z o.o. PL-AR-000002989

Other devices from Zhuji Pengtian Medical Instrument Co., Ltd.

See all devices from Zhuji Pengtian Medical Instrument Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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