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Gs Cuff Ss (hxa-Gcuff-Sslb)

EUDAMED

Class I (EU MDR)

Ref HXA-GCUFF-SSLB

by OMRON Healthcare Co., Ltd.

Identity

Trade Name
GS CUFF SS (HXA-GCUFF-SSLB) EUDAMED
Device Name
GS CUFF SS EUDAMED
Model / Reference
HXA-GCUFF-SSLB EUDAMED

Identifiers

Primary DI / UDI-DI
04015672107267 EUDAMED
Basic UDI-DI
4015672107265K EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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 Ss (hxa-Gcuff-Sslb) 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 7975e502-8283-4fc6-9be3-ee6be1f6153d 61 fields · synced Oct 5, 2026