Skip to content

spineshape

by SpineSave AG Switzerland EUDAMED

Ref 20.010.05 EMDN L0922

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260682510495 Basic UDI-DIDate24 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
BLUNT WIRE d 1.6
Model / Reference
20.010.05
Primary DI / UDI-DI
04260682510495
Basic UDI-DI
B-04260682510495
EMDN Code
L0922 Orthopaedic surgery guides, 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 53c73941-7b5e-4009-aa2a-747ae46f4390 61 fields · synced 25 Oct 2026