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Vanocathe

by iLife Medical Devices Pvt Ltd 28 variants

Ref 907.06.01.00Model Measure Volume Set

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890603910907G3 Basic UDI-DI 08906039101683UDI-DIDate28 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
Measure Volume Set, 907.06.01.00
Primary DI / UDI-DI
08906039101683
Basic UDI-DI
890603910907G3
EMDN Code
A03010199 Infusion controllers - other
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IN-MF-000014372
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from iLife Medical Devices Pvt Ltd

See all devices from iLife Medical Devices Pvt Ltd →

Properties

  • Sterile
  • Contains Latex
  • Measuring Function

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No