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I., PROMAX, AG, 2N protiskluz.lem, černá

EUDAMED

Class I (EU MDR)

Ref 8591285279912

by MAXIS a.s.

Identity

Trade Name
I.,PROMAX,AG,2N protiskluz.lem,černá EUDAMED
Device Name
Kompresní punčochy PROMAX Standard I.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285279912 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285279912 EUDAMED
Basic UDI-DI
8591285AGLP12D EUDAMED
EMDN Code
M030405 COMPRESSION STOCKINGS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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: Compression/pressure sock/stocking, single-use

I., PROMAX, AG, 2N protiskluz.lem, černá by MAXIS a.s. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
MAXIS a.s.
EUDAMED SRN
CZ-MF-000000989

Sources (1)

  • EUDAMED 0a1fd3d3-fa05-4ee3-868a-c4e69d7eb946 61 fields · synced Jun 20, 2026