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Kit de Infusión Personalizado (Reservorio 100 ml / 4 vías - 9 mm)

by Laboratorios Grifols, S.A.

Ref 736860

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 Number8437017294A030001LT Basic UDI-DI 08437017294498UDI-DIDate8 Sep 2025RegisteredStatusActive

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  • Withdrawn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 de Infusión Personalizado
Model / Reference
736860
Primary DI / UDI-DI
08437017294498
Basic UDI-DI
8437017294A030001LT
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class IIa
Medical Purpose
Kit para administración subcutánea de medicamentos.

Manufacturer details

EUDAMED SRN
ES-PR-000048778

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Properties

Other properties (1)

  • Sterile: No