Skip to content

SPS® HA - Size F / Side RIGHT

by Symbios Orthopédie S.A.

Ref 3022 0600

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-07630013603887 Basic UDI-DI 07630013603887UDI-DIDate15 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
SPS® HA - Size F / Side RIGHT
Model / Reference
3022 0600
Primary DI / UDI-DI
07630013603887
Basic UDI-DI
B-07630013603887
EMDN Code
P090804010202 Uncemented femoral stems for primary implant, with fixed neck, anatomical
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000020168
Authorised representative
Symbios France SAS FR-AR-000017731

Other devices from Symbios Orthopédie S.A.

See all devices from Symbios Orthopédie S.A. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No