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Amifil M

by Spółdzielnia Niewidomych SINPO 51 variants

Ref 580456Model Amifil M 2MA 404PK 4-0 CE-4F

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 Number59043890107024S Basic UDI-DI Date23 Sep 2022RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
NICI CHIRURGICZNE sterylne, monofilowe Amifil M 2MA 404PK 4-0 CE-4F 1 saszetka
NICI CHIRURGICZNE sterylne, monofilowe Amifil M 2MA 404PK 4-0 CE-4F karton zbiorczy
Model / Reference
Amifil M 2MA 404PK 4-0 CE-4F, 580456
Primary DI / UDI-DI
05904389010702, 05904389010726
Basic UDI-DI
59043890107024S, 590438901072658
Direct Marketing DI
05904389010719
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