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II., PROMAX, AD, 7N, tělová

EUDAMED

Class I (EU MDR)

Ref 8591285281380Ref 8591285084721

by MAXIS a.s.

Identity

Trade Name
II.,PROMAX,AD,7N,tělová EUDAMED
II.,S,PROMAX,AD,7N,tělová EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Lýtková punčocha EUDAMED
Model / Reference
8591285281380 EUDAMED
8591285084721 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285281380 EUDAMED
08591285084721 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

II., PROMAX, AD, 7N, 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 23ea3c5f-df0e-42ae-b53e-a136ae2b7b6a 61 fields · synced Jul 20, 2026
  • EUDAMED 5dab1196-7514-4ce4-8548-0eac1ea24b38 61 fields · synced May 18, 2026