Skip to content

Protector Pad Pour Elevating and Articulating Legrest - Right

by Les Equipements Adaptés PHYSIPRO INC

Ref MI7575-R

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++G094PHYLOWERLIMBSDN Basic UDI-DIDate6 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Phylowerlimbs
Model / Reference
MI7575-R
Primary DI / UDI-DI
+G094MI7575R0W
Basic UDI-DI
++G094PHYLOWERLIMBSDN
EMDN Code
Y180980 Seating systems / posture systems / seating aids - accessories
Device Class
Class I
Market of Registration
France

Manufacturer details

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

Other devices from Les Equipements Adaptés PHYSIPRO INC

See all devices from Les Equipements Adaptés PHYSIPRO INC →

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