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I., PROMAX, AG, 2+K protIskluz.lem, černá

EUDAMED

Class I (EU MDR)

Ref 8591285280215Ref 8591285280857

by MAXIS a.s.

Identity

Trade Name
I.,PROMAX,AG,2+K protIskluz.lem,černá EUDAMED
I.,S,PROMAX,AG,2+K protIskluz.lem,černá EUDAMED
Device Name
Kompresní punčochy PROMAX Standard I.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285280215 EUDAMED
8591285280857 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285280215 EUDAMED
08591285280857 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

I., PROMAX, AG, 2+K protIskluz.lem, černá by MAXIS a.s. — 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

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

Sources (2)

  • EUDAMED ba4cc624-ba33-4504-9cce-a67d12d090b0 61 fields · synced Jul 25, 2026
  • EUDAMED f9a468e3-ad9a-4b9b-9288-5e9f404cdcf7 61 fields · synced May 19, 2026