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Gs Cuff2 M (hxa-Gcfm-Pbe)

EUDAMED

Class I (EU MDR)

Ref HXA-GCFM-PBE

by OMRON Healthcare Co., Ltd.

Identity

Trade Name
GS CUFF2 M (HXA-GCFM-PBE) EUDAMED
Device Name
GS CUFF2 M EUDAMED
Model / Reference
HXA-GCFM-PBE EUDAMED

Identifiers

Primary DI / UDI-DI
04015672111561 EUDAMED
Basic UDI-DI
40156721115655 EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Gs Cuff2 M (hxa-Gcfm-Pbe) by OMRON Healthcare Co., Ltd. — 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
JP-MF-000007213
Authorised Representative
OMRON Healthcare Europe B.V. NL-AR-000002683

Sources (1)

  • EUDAMED 33e3831a-2e0b-4584-b0ca-ba20256da5a6 61 fields · synced Jun 20, 2026