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Gs Cuff Xl (hxa-Gcuff-Xllb)

EUDAMED

Class I (EU MDR)

Ref HXA-GCUFF-XLLB

by OMRON Healthcare Co., Ltd.

Identity

Trade Name
GS CUFF XL (HXA-GCUFF-XLLB) EUDAMED
Device Name
GS CUFF XL EUDAMED
Model / Reference
HXA-GCUFF-XLLB EUDAMED

Identifiers

Primary DI / UDI-DI
04015672107229 EUDAMED
Basic UDI-DI
4015672107225B EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Hungary 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 Cuff Xl (hxa-Gcuff-Xllb) 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 9ee88a00-340b-485f-8942-39a15a48ca43 61 fields · synced Oct 7, 2026