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HP2 - CONTOUR BACKREST (STANDARD) - 22" x 24" (559 x 610 MM)

by Les Equipements Adaptés PHYSIPRO INC

Ref HPC2224

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 Number++G094PHYBACKRESTNV Basic UDI-DI +G094HPC222405UDI-DIDate7 Aug 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  • Withdrawn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
Phybackrest
Model / Reference
HPC2224
Primary DI / UDI-DI
+G094HPC222405
Basic UDI-DI
++G094PHYBACKRESTNV
EMDN Code
Y180980 Seating systems / posture systems / seating aids - accessories
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CA-MF-000024015
Authorised representative
S4M EUROPE FR-AR-000000180

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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