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Canwell

by Canwell Medical Co., Ltd. 1,000+ variants

Ref 232536750

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-06942980249212 Basic UDI-DI 06942980249212UDI-DIDate10 Oct 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Spinal Fixation Systems
Model / Reference
232536750
Primary DI / UDI-DI
06942980249212
Basic UDI-DI
B-06942980249212
EMDN Code
P09070302 Thoracolumbosacral fixation systems
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
CN-MF-000025329
Authorised representative
Llins Service & Consulting GmbH DE-AR-000009077

Other devices from Canwell Medical Co., Ltd

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  • Canwell

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  • Canwell

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  • Canwell

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See all devices from Canwell Medical Co., Ltd →

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