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Capd Szett Diaverum A1

by TZMO Hungary Kft

Ref NM-XXX-XXXX-246

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 Number59983223DDMXXXX89 Basic UDI-DI 05998322310028UDI-DIDate21 May 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  • Withdrawn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 - Hu
Model / Reference
NM-XXX-XXXX-246
Primary DI / UDI-DI
05998322310028
Basic UDI-DI
59983223DDMXXXX89
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Medical Purpose
This set is a compilation of defined components used together to perform medical care.

Manufacturer details

EUDAMED SRN
HU-PR-000009254

Related devices

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

Properties

Other properties (1)

  • Sterile: No