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Baguera® L Intersomatic Distractor

by Spineart SA

Ref LIN-00 00 02-N

Active European Union

CE MDR

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/MDR Number1764045086SRI00REUSIN1R3E Basic UDI-DI 07640139343550UDI-DIDate25 Jun 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
SURGICAL REUSABLE INSTRUMENTS Ir
Model / Reference
LIN-00 00 02-N
Primary DI / UDI-DI
07640139343550
Basic UDI-DI
1764045086SRI00REUSIN1R3E
Direct Marketing DI
07640139343550
EMDN Code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000015664
Authorised representative
Alpes CN SAS FR-AR-000013241

Other devices from Spineart

See all devices from Spineart →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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