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Minisart® NML | Ophthalsart

by Sartorius Stedim Biotech GmbH EUDAMED

Active European Union

Ref 16555--------GUKModel Minisart® NML | Ophthalsart

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4063233MISFCA045MBSYEGA9W Basic UDI-DIDate24 Jun 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Minisart® NML | Ophthalsart, 16555--------GUK
Primary DI / UDI-DI
04063233000656
Basic UDI-DI
4063233MISFCA045MBSYEGA9W
EMDN Code
A04010101 Withdrawl and administration filters (0.2-1.2 microns)
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000017607

Other devices from Sartorius Stedim Biotech GmbH

See all devices from Sartorius Stedim Biotech GmbH →

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