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II., S, PROMAX, AD, 5N, černá

EUDAMED

Class I (EU MDR)

Ref 8591285281632Ref 8591285281311

by MAXIS a.s.

Identity

Trade Name
II.,S,PROMAX,AD,5N,černá EUDAMED
II.,PROMAX,AD,5N,černá EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Lýtková punčocha EUDAMED
Model / Reference
8591285281632 EUDAMED
8591285281311 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285281632 EUDAMED
08591285281311 EUDAMED
Basic UDI-DI
8591285ADP267 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, AD, 5N, 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 (2)

  • EUDAMED 5673493d-eed5-43bb-9393-1910caf53e1f 61 fields · synced Jul 25, 2026
  • EUDAMED b80efd05-9c01-4946-a21f-7cabd26b6278 61 fields · synced May 18, 2026