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KIT AUTONOMIE 20mL

by Lfb Biomedicaments

Ref 38117Model KIT AUTONOMIE

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3700386800017V Basic UDI-DI 03700386801136UDI-DIDate26 Dec 2024RegisteredStatusActive

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  • Withdrawn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
Kit Autonomie
Model / Reference
KIT AUTONOMIE, 38117
Primary DI / UDI-DI
03700386801136
Basic UDI-DI
3700386800017V
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class IIa
Medical Purpose
Administration des facteurs de coagulation de LFB BIOMEDICAMENTS

Manufacturer details

EUDAMED SRN
FR-PR-000043590

Other devices from Lfb Biomedicaments

Properties

Other properties (1)

  • Sterile: No