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Poseidon Hydrophilic Nitinol Guide Wire

by SP Medical A/S 197 variants

Ref HY-N-A-ST-035-D-210

Expiring European Union

CE MDR

Valid until

6 Jul 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV Rheinland LGA Products GmbH

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 Number5710086-GWPOLZ Basic UDI-DI 05710086003691UDI-DIDate12 May 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Poseidon Hydrophilic Guide Wire
Model / Reference
HY-N-A-ST-035-D-210
Primary DI / UDI-DI
05710086003691
Basic UDI-DI
5710086-GWPOLZ
EMDN Code
C04010201 Coronary artery therapeutic guidewires, hydrophilic
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DK-MF-000019782

Other devices from SP Medical A/S

See all devices from SP Medical A/S →

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