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OneFlon

by iLife Medical Devices Pvt Ltd 29 variants

Ref 904.01.01.00Model Blood Transfusion Set (Vented & Non Vented)

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890603910904FV Basic UDI-DI 08906039101508UDI-DIDate5 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  • Withdrawn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

Device Name
Blood Transfusion Set
Model / Reference
Blood Transfusion Set (Vented & Non Vented), 904.01.01.00
Primary DI / UDI-DI
08906039101508
Basic UDI-DI
890603910904FV
EMDN Code
Z121799 Blood transfusion instruments - 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

Other properties (11)

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