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EQSens Flow with vertical measuring cloumn

by Medicop - specialna oprema d.o.o.

Ref IZ08389_EQSens_FLOW_COLUMN_ENModel EQSens Flow

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3838578EQUSPEGFM788192P6C Basic UDI-DI 93838578000739UDI-DIDate12 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  • Withdrawn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
Flowmeter
Model / Reference
EQSens Flow, IZ08389_EQSens_FLOW_COLUMN_EN
Primary DI / UDI-DI
93838578000739
Basic UDI-DI
3838578EQUSPEGFM788192P6C
Direct Marketing DI
93838578000739
EMDN Code
A030104 Flow regulators
Device Class
Class IIa
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000002144

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Properties

  • Administering Medicine
  • Measuring Function

Other properties (11)

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