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Pressio® 3 – Patientenmonitor-Verlängerungskabel – 3 Parameter (Icp, Ict, Map)

by Sophysa

Ref PSO-MPM01

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376012413PSOMPM01XH Basic UDI-DI 03760409449660UDI-DIDate10 Oct 2025RegisteredStatusActive

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  • Withdrawn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
Pressio 3 - Patient Monitor Extension Cable
Model / Reference
PSO-MPM01
Primary DI / UDI-DI
03760409449660
Basic UDI-DI
376012413PSOMPM01XH
Direct Marketing DI
03760409449660
EMDN Code
Z12039099 Various instruments to support and monitor vital signs – other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000002870

Other devices from Sophysa

See all devices from Sophysa →

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