Skip to content

Huber Infusion Set without safety

by Poly Medicure Limited India EUDAMED

Ref 95017Model Huber Infusion Set without safety

EMDN A01010302

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890209595010GU Basic UDI-DIDate21 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Huber Infusion set with/without safety
Model / Reference
Huber Infusion Set without safety, 95017
Primary DI / UDI-DI
08902095950173
Basic UDI-DI
890209595010GU
EMDN Code
A01010302 Needles and kits for implantable systems (port), w/o safety systems
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IN-MF-000003380
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Poly Medicure Limited

See all devices from Poly Medicure Limited →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Administering Medicine
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 08902095950173|890209595010GU 61 fields · synced 24 Oct 2026