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Meropenem-vaborbactam (20+10) M/V 30 µg

by Liofilchem S.r.l. EUDAMED

Active European Union

Ref 9326/1

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number805518287ATBDISC326Z5 Basic UDI-DIDate16 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Meropenem-vaborbactam (20+10) M/V 30 µg
Model / Reference
9326/1
Primary DI / UDI-DI
08058951161976
Basic UDI-DI
805518287ATBDISC326Z5
EMDN Code
W0104080502 Impregnated disks, multi-disks & tablets
Device Class
Class B
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000026495

Other devices from Liofilchem S.r.l.

See all devices from Liofilchem S.r.l. →

Properties

Show properties
  • Professional Testing
Other properties (10)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No