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spineshape

by SpineSave AG Switzerland EUDAMED

Ref 20.003.10

EMDN L091103

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260682510327 Basic UDI-DIDate24 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Distraction Forceps
Model / Reference
20.003.10
Primary DI / UDI-DI
04260682510327
Basic UDI-DI
B-04260682510327
EMDN Code
L091103 Orthopaedic prostheses forceps, reusable
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000041640
Authorised representative
SpineSave GmbH DE-AR-000023363

Other devices from SpineSave AG

See all devices from SpineSave AG →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
Other properties (10)
  • Sterile: No
  • Implantable: 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

Sources (1)

  • EUDAMED bc09f774-c5fa-41be-bb39-1736767ffbda 61 fields · synced 24 Oct 2026