Skip to content

Xtern Frontier Anterior Foot Drop Orthotic Size Medium

by Turbomed Orthotics inc.

Ref 102100-SA-M

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number62846468102100VF Basic UDI-DI 00628464680042UDI-DIDate11 Mar 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  • Withdrawn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
Xtern Frontier Anterior Foot Drop Orthotic
Model / Reference
102100-SA-M
Primary DI / UDI-DI
00628464680042
Basic UDI-DI
62846468102100VF
EMDN Code
Y06120602 Energy return ankle-foot orthoses
Device Class
Class I
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
CA-MF-000032108
Authorised representative
OKO SOLUTION FR-AR-000006781

Other devices from Turbomed Orthotics inc.

See all devices from Turbomed Orthotics 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