Skip to content

Pro-Omnia Lock

by Pro-Active S.R.L. 2 variants

Ref MF005BModel PRO-OMNIA LOCK

Active European Union

CE MDR

Valid until

27 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ICIM S.P.A.

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 Number803402827MFQJ Basic UDI-DI 18034028276245UDI-DIDate8 Oct 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030220-00 Active

    Quality assurance EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    28 Sep 2026
    Expires
    27 Sep 2031

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
PRO-OMNIA LOCK, MF005B
Primary DI / UDI-DI
18034028276245
Basic UDI-DI
803402827MFQJ
Unit of Use DI
08034028276248
EMDN Code
A07050202 Caps or obturators, perforable without needle
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000028985

Other devices from Pro-Active S.R.L.

  • Infu-Pro

    Class I

  • 3-Way Pro

    Class I

  • Uro-Pro

    Class I

  • Pro-Long Tube

    Class I

  • Buret-Pro

    Class I

  • Pro-Omnia Lock

    Class I

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No