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Miniflow

EUDAMED

Class IIa (EU MDR)

Ref BM4000SLE

by medin Medical Innovations GmbH

Identity

Device Name
Miniflow EUDAMED
Model / Reference
BM4000SLE EUDAMED

Identifiers

Primary DI / UDI-DI
04060139050013 EUDAMED
Basic UDI-DI
4060139000042H EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Pulmonary function analysis system, adult

Miniflow by medin Medical Innovations GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006975

Sources (1)

  • EUDAMED 08486dda-7a44-450e-871f-369136bce87c 61 fields · synced Jul 9, 2026