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Rhizorthese

by Orthosoft 6 variants

Ref RH13GModel RHIZORTHESE

Rhizorthese (RH13G) is a Class I device made by Orthosoft, registered in EUDAMED on 15 Feb 2022 (Basic UDI-DI 37602703434010774567J), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37602703434010774567J Basic UDI-DI 03760270340288UDI-DIDate15 Feb 2022RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
RHIZORTHESE, RH13G
Primary DI / UDI-DI
03760270340288
Basic UDI-DI
37602703434010774567J
EMDN code
Y060606 Hand orthoses
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000216

Similar devices in this category

Other devices filed under UPPER EXTREMITY ORTHOSES (SPLINTS AND BRACES).

Other devices from Orthosoft

See all devices from Orthosoft →

Properties

Other properties (14, all answered No)