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Amifil M

by Spółdzielnia Niewidomych "SINPO" EUDAMED

Withdrawn Not intended for the EU market

Ref 580501Model Amifil M 2MO 404 4-0 CE-3

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59043890103444N Basic UDI-DIDate6 Oct 2022RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
NICI CHIRURGICZNE sterylne, monofilowe Amifil M 2MO 404 4-0 CE-3 1 saszetka
Model / Reference
Amifil M 2MO 404 4-0 CE-3, 580501
Primary DI / UDI-DI
05904389010344
Basic UDI-DI
59043890103444N
EMDN Code
H010201010101 Polyamide monofilament with needle
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
PL-MF-000004331

Properties

  • Sterile

Other properties (12)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No