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ProInject syringe

by Margomed Spółka Akcyjna Poland EUDAMED

Ref 010 210Model LuxInject syringe, ProInject syringe

EMDN A020199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59045539930101WA Basic UDI-DIDate10 Sep 2025RegisteredStatusActive

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
Syringe
Model / Reference
LuxInject syringe, ProInject syringe, 010 210
Primary DI / UDI-DI
05905386929325
Basic UDI-DI
59045539930101WA
EMDN Code
A020199 Syringes, single-use - other
Device Class
Class IIa
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000009261

Other devices from Margomed Spółka Akcyjna

See all devices from Margomed Spółka Akcyjna →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Measuring Function
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
  • Administering Medicine: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 05905386929325|59045539930101WA 61 fields · synced 24 Oct 2026