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Single-patient-cuff large adult

EUDAMED

Class I (EU MDR)

Ref 04.85140.241

by Kirchner & Wilhelm GmbH + Co KG

Identity

Trade Name
Single-patient-cuff large adult EUDAMED
Device Name
Aneroid sphygmomanometers EUDAMED
Model / Reference
04.85140.241 EUDAMED

Identifiers

Primary DI / UDI-DI
04030155018823 EUDAMED
Basic UDI-DI
4030155KaWe04SQ EUDAMED
EMDN Code
C9006 ANEROID SPHYGMOMANOMETERS EUDAMED

Classification

Device Class
Class I 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Single-patient-cuff large adult by Kirchner & Wilhelm GmbH + Co KG — Class I — 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
DE-MF-000006338

Sources (1)

  • EUDAMED 41157295-206e-4d27-8274-22768bf02c8e 61 fields · synced Jul 11, 2026