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Azot

EUDAMED

Class I (EU MDR)

Ref AZ-803P

by Lu Mark Healthcare Co., Ltd.

Identity

Trade Name
AZOT EUDAMED
Device Name
Cold Compression Therapy for Ankle EUDAMED
Model / Reference
AZ-803P EUDAMED

Identifiers

Primary DI / UDI-DI
04719879060393 EUDAMED
Basic UDI-DI
471987906A015E4 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Category: Hot/cold therapy pack, reusable

Azot by Lu Mark Healthcare Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TW-MF-000015951
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED c8844599-b48e-4c0e-aaa9-9e7ccdacf795 61 fields · synced Jun 18, 2026