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Arterial Hemostasis Compressor

EUDAMED

Class I (EU MDR)

Ref 239410Model N8040, N10040, NP12040, NP16040, TP16040, TP20040

by Hubei MeterOmega Technology LTD

Identity

Device Name
Arterial Hemostasis Compressor EUDAMED
Model / Reference
N8040, N10040, NP12040, NP16040, TP16040, TP20040 EUDAMED
239410 EUDAMED

Identifiers

Primary DI / UDI-DI
06974617175557 EUDAMED
Basic UDI-DI
697461717301LK EUDAMED
EMDN Code
M040599 HAEMOSTATIC DRESSINGS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

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

Arterial Hemostasis Compressor by Hubei MeterOmega Technology 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
CN-MF-000016732
Authorised Representative
Humiss Beratung GmbH DE-AR-000023447

Sources (1)

  • EUDAMED 6bd83254-b363-4983-a1f8-bd36fd3df79a 61 fields · synced Jun 18, 2026