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II., S, PROMAX, AG, 3+K protiskluz.lem, tělová

EUDAMED

Class I (EU MDR)

Ref 8591285085278Ref 8591285282806

by MAXIS a.s.

Identity

Trade Name
II.,S,PROMAX,AG,3+K protiskluz.lem,tělová EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285085278 EUDAMED
8591285282806 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285085278 EUDAMED
08591285282806 EUDAMED
Basic UDI-DI
8591285AGLP22F 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

II., S, PROMAX, AG, 3+K protiskluz.lem, tělová 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 813a0ae0-2163-4626-8b92-506038db9da9 61 fields · synced Oct 5, 2026
  • EUDAMED 344e849e-500e-4c35-a1f0-81a6bd20ed28 61 fields · synced May 19, 2026