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II., PROMAX, AG, 6N protiskluz.lem, tělová

EUDAMED

Class I (EU MDR)

Ref 8591285084868Ref 8591285282622Ref 8591285085025Ref 8591285281984

by MAXIS a.s.

Identity

Trade Name
II.,PROMAX,AG,6N protiskluz.lem,tělová EUDAMED
II.,S,PROMAX,AG,6N protiskluz.lem,tělová EUDAMED
II.,PROMAX,AG,6+N protiskluz.lem,tělová EUDAMED
Device Name
Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
Model / Reference
8591285084868 EUDAMED
8591285282622 EUDAMED
8591285085025 EUDAMED
8591285281984 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285084868 EUDAMED
08591285282622 EUDAMED
08591285085025 EUDAMED
08591285281984 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., PROMAX, AG, 6N protiskluz.lem, tělová 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 (4)

  • EUDAMED 8a5eca4a-0477-4aa9-8b9d-4a3cc7c8ac7a 61 fields · synced Jul 31, 2026
  • EUDAMED 802637f0-e639-47db-a142-e3d4befaf50d 61 fields · synced May 18, 2026
  • EUDAMED 9a36d5d6-580a-4494-b0a6-e4f882163339 61 fields · synced May 18, 2026
  • EUDAMED f6c20dd5-0c33-424e-9158-8c734c342230 61 fields · synced May 19, 2026