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Matoset

by Toruńskie Zakłady Materiałów Opatrunkowych Spółka Akcyjna 135 variants

Ref MN-991-MIXX-135

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, self-declared

Class I: no certifier involved

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 Number5900516BBRXXXXXQ Basic UDI-DI 05900516345464UDI-DIDate5 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

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  • Withdrawn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-135
Primary DI / UDI-DI
05900516345464
Basic UDI-DI
5900516BBRXXXXXQ
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
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