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Matoset

by Toruńskie Zakłady Materiałów Opatrunkowych Spółka Akcyjna 51 variants

Ref MN-991-MIXX-066

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5900516FFMXXXXZR Basic UDI-DI 05900516328603UDI-DIDate4 Mar 2026RegisteredStatusWithdrawn No longer placed 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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
System/Procedure Pack
Model / Reference
MN-991-MIXX-066
Primary DI / UDI-DI
05900516328603
Basic UDI-DI
5900516FFMXXXXZR
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
Medical Purpose
A Matoset is the compilation of defined components used together to perform medical care.

Manufacturer details

EUDAMED SRN
PL-PR-000002201

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Category: Ophthalmic surgical procedure kit, non-medicated, single-use

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Properties

Other properties (1)

  • Sterile: No