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Contactboard-GO, 1-fold - FX

by CODAN pvb Critical Care GmbH 10 variants

Ref 75.1193Model Zubehör / Accessory IBPM

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4046765CABFXBMB Basic UDI-DI 04046765105440UDI-DIDate27 May 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  • Withdrawn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
Electrical Reusable Equipment FX - Xtrans®/DPT-9000
Model / Reference
Zubehör / Accessory IBPM, 75.1193
Primary DI / UDI-DI
04046765105440
Basic UDI-DI
4046765CABFXBMB
EMDN Code
Z1203020301 Invasive blood pressure monitoring instruments
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
DE-MF-000007510

Other devices from CODAN pvb Critical Care GmbH

See all devices from CODAN pvb Critical Care GmbH →

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