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Pressure Infusion Bag

by Noxa Medical Oü Estonia EUDAMED

Ref 500ml,1000ml,3000ml, 5000ml EMDN A0303

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number47450110397NCZP Basic UDI-DIDate25 Jun 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Reusable Pressure Infusion Bag
Model / Reference
500ml, 1000ml, 3000ml, 5000ml
Primary DI / UDI-DI
04745011039729
Basic UDI-DI
47450110397NCZP
Direct Marketing DI
04745011039729
EMDN Code
A0303 Rapid infusion systems (high flow)
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
EE-MF-000042213

Other devices from Noxa Medical Oü

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
Other properties (12)
  • Sterile: No
  • Implantable: No
  • Contains Latex: 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

Sources (1)

  • EUDAMED 27cc6c28-d5eb-42e0-aadb-732ee92c774d 61 fields · synced 22 Oct 2026