← Back to catalogue
II., S, PROMAX, AG, 4K protiskluz.lem, tělová
EUDAMEDClass I (EU MDR)
Ref 8591285282523Ref 8591285084813
by MAXIS a.s.
Identity
- Trade Name
- II.,S,PROMAX,AG,4K protiskluz.lem,tělová EUDAMEDII.,PROMAX,AG,4K protiskluz.lem,tělová EUDAMED
- Device Name
- Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
- Model / Reference
- 8591285282523 EUDAMED8591285084813 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285282523 EUDAMED08591285084813 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
II., S, PROMAX, AG, 4K protiskluz.lem, 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8591285AGLP22F | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- MAXIS a.s.
- EUDAMED SRN
- CZ-MF-000000989
Sources (2)
- EUDAMED 4c181381-762e-489f-ba7b-3f47f6ff866c 61 fields · synced Jul 23, 2026
- EUDAMED 08b882e1-b92f-4b59-9979-81450d1dd947 61 fields · synced May 18, 2026