← Back to catalogue

Blutdruckmessgerät aneroid / Blood press

EUDAMED

Class I (EU MDR)

Ref 34101-03

by REDA Instrumente GmbH

Identity

Device Name
Blutdruckmessgerät aneroid / Blood press EUDAMED
Model / Reference
34101-03 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058028545 EUDAMED
Basic UDI-DI
4063058000001243N EUDAMED
Direct Marketing DI
04063058028545 EUDAMED
EMDN Code
Z12050501 CARDIAC OUTPUT MEASUREMENT METERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Blutdruckmessgerät aneroid / Blood press by REDA Instrumente GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005592

Sources (1)

  • EUDAMED 240f9deb-753e-4014-be06-48a8b0ec64cf 61 fields · synced Jun 11, 2026