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SG13-40

by Animus Beyford Trading Sl

Ref SG13-40Model Laringo-Tracheo-Bronchial Prosthesis and Tubes

Active European Union

CE MDR

Valid until

16 Jun 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0030250126 Date4 Jun 2026IssuedStatusActive expires 16 Jun 2030

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Laringo-Tracheo-Bronchial Prosthesis and Tubes, SG13-40
Primary DI / UDI-DI
08435544701106
Basic UDI-DI
84355447LTBPTV2
EMDN Code
P0401 Tracheobronchial prostheses
Device Class
Class IIb
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000030308

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See all devices from Animus Beyford Trading Sl →

Properties

  • Sterile
  • Implantable

Other properties (12)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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