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DanFlow 1000

EUDAMED

Class IIa (EU MDR)

Ref MU1002

by MEDKONSULT medical technology s.r.o.

Identity

Trade Name
DanFlow 1000 EUDAMED
Device Name
DANFLOW EUDAMED
Model / Reference
MU1002 EUDAMED

Identifiers

Primary DI / UDI-DI
08594211570015 EUDAMED
Basic UDI-DI
859421157DANFLOWPS EUDAMED
EMDN Code
Z121605 UROFLOWMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

DanFlow 1000 by MEDKONSULT medical technology s.r.o. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CZ-MF-000016193

Sources (1)

  • EUDAMED 8f07c055-ce33-4d4e-aba1-ab8647a582d9 61 fields · synced Jun 18, 2026