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Humerus Nail Cannulated 08 MM

by Nebula Surgical Private Limited EUDAMED

Withdrawn No longer placed on the EU market

Ref 154.C08.25

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08905827007572 Basic UDI-DIDate16 Sep 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

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.

Specification

EUDAMED

Device Name
IM Nail Cannulated (SS)
Model / Reference
154.C08.25
Primary DI / UDI-DI
08905827007572
Basic UDI-DI
B-08905827007572
EMDN Code
P09120201 Intramedullary nails
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IN-MF-000026763
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Nebula Surgical Private Limited

See all devices from Nebula Surgical Private Limited →

Properties

  • Implantable

Other properties (12)

  • Sterile: 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