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II., S, PROMAX, AG, 1+N protiskluz.lem, černá

EUDAMED

Class I (EU MDR)

Ref 8591285282752Ref 8591285282110

by MAXIS a.s.

Identity

Trade Name
II.,S,PROMAX,AG,1+N protiskluz.lem,černá EUDAMED
II.,PROMAX,AG,1+N protiskluz.lem,černá EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285282752 EUDAMED
8591285282110 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285282752 EUDAMED
08591285282110 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, 1+N 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 cc768331-4bb0-48cf-9043-4d0b7eb80087 61 fields · synced Jul 23, 2026
  • EUDAMED 890264a3-125b-43cf-b152-5f8180643398 61 fields · synced May 19, 2026