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Matoset

by Toruńskie Zakłady Materiałów Opatrunkowych Spółka Akcyjna 51 variants

Ref MN-991-MIXX-120

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 Number5900516FFMXXXXZR Basic UDI-DI 05900516338114UDI-DIDate4 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  • Withdrawn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-120
Primary DI / UDI-DI
05900516338114
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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Properties

Other properties (1)

  • Sterile: No