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Set 3

by OneMed Oy 3 variants

Ref Set 3

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6429830H02CW Basic UDI-DI 06429830066125UDI-DIDate4 Apr 2025RegisteredStatusActive

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  • Withdrawn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
Set 3
Model / Reference
Set 3
Primary DI / UDI-DI
06429830066125
Basic UDI-DI
6429830H02CW
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
Medical Purpose
Set of single use first aid medical devices

Manufacturer details

EUDAMED SRN
FI-PR-000046441

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from OneMed Oy

Properties

Other properties (1)

  • Sterile: No