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Oscimed Psv II

by Oscimed SA 8 variants

Ref OSC 400Model Cast cutter saw

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 Number764010492PLASTERSAWEV Basic UDI-DI 07640104924005UDI-DIDate8 Nov 2022RegisteredStatusActive

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  • Withdrawn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
Plaster Saw
Model / Reference
Cast cutter saw, OSC 400
Primary DI / UDI-DI
07640104924005
Basic UDI-DI
764010492PLASTERSAWEV
EMDN Code
Z12139005 Plaster cast saws
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CH-MF-000009605
Authorised representative
OSCIMED EUROPE SAS FR-AR-000028943

Other devices from Oscimed SA

See all devices from Oscimed SA →

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