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II., S, PROMAX, AG, 5K protiskluz.lem, černá
EUDAMEDClass I (EU MDR)
Ref 8591285282578Ref 8591285281939
by MAXIS a.s.
Identity
- Trade Name
- II.,S,PROMAX,AG,5K protiskluz.lem,černá EUDAMEDII.,PROMAX,AG,5K protiskluz.lem,černá EUDAMED
- Device Name
- Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
- Model / Reference
- 8591285282578 EUDAMED8591285281939 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285282578 EUDAMED08591285281939 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, 5K 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.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8591285AGLP22F | Class I | Active |
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Manufacturer
- Manufacturer
- MAXIS a.s.
- EUDAMED SRN
- CZ-MF-000000989
Sources (2)
- EUDAMED 3b31ad32-ff04-4122-8acd-c623630ad91d 61 fields · synced Jul 11, 2026
- EUDAMED a0ea333b-b71d-46a1-9793-377bef745767 61 fields · synced May 18, 2026