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SET A 2 VALVOLE NEEDLE FREE PER FARMACI CHEMIOTERAPICI TUBO PUR, RUBINETTO con VALVOLA NEEDLE FREE PER BOLI

by Meika Group S.r.l.

Ref MUL5375Model MULTIFLEX

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-08055348432381 Basic UDI-DI 08055348432381UDI-DIDate5 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
SET A 2 VALVOLE NEEDLE FREE PER FARMACI CHEMIOTERAPICI TUBO PUR, RUBINETTO con VALVOLA NEEDLE FREE PER BOLI
Model / Reference
MULTIFLEX, MUL5375
Primary DI / UDI-DI
08055348432381
Basic UDI-DI
B-08055348432381
EMDN Code
A03010199 Infusion controllers - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029106

Other devices from Meika Group S.r.l.

See all devices from Meika Group S.r.l. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No