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Hxa-Gcfss-Pbap

EUDAMED

Class I (EU MDR)

Ref HXA-GCFSS-PBAP

by OMRON Healthcare Co., Ltd.

Identity

Device Name
HXA-GCFSS-PBAP EUDAMED
Model / Reference
HXA-GCFSS-PBAP EUDAMED

Identifiers

Primary DI / UDI-DI
04975479496448 EUDAMED
Basic UDI-DI
497547949644QA EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I 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

Hxa-Gcfss-Pbap 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 9a99684f-7593-42b3-842d-134bd2a17adf 61 fields · synced Oct 6, 2026