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Matoset

by Toruńskie Zakłady Materiałów Opatrunkowych Spółka Akcyjna 25 variants

Ref MN-991-MIXX-122

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5900516EEJXXXXXS Basic UDI-DI 05900516340605UDI-DIDate5 Mar 2026RegisteredStatusActive

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  • Withdrawn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
System/Procedure Pack
Model / Reference
MN-991-MIXX-122
Primary DI / UDI-DI
05900516340605
Basic UDI-DI
5900516EEJXXXXXS
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIb
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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Properties

Other properties (1)

  • Sterile: No