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

EUDAMED

Class I (EU MDR)

Ref 8591285282431

by MAXIS a.s.

Identity

Trade Name
II.,S,PROMAX,AG,1N protiskluz.lem,černá EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285282431 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285282431 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

Category: Compression/pressure sock/stocking, single-use

II., S, PROMAX, AG, 1N 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 373ffd9b-a7e2-4e20-b46e-dfe311396d91 61 fields · synced Jun 18, 2026