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II., S, PROMAX, AG, 4+K protiskluz.lem, tělová
EUDAMEDClass I (EU MDR)
Ref 8591285282844Ref 8591285281885Ref 8591285085292
by MAXIS a.s.
Identity
- Trade Name
- II.,S,PROMAX,AG,4+K 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
- 8591285282844 EUDAMED8591285281885 EUDAMED8591285085292 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285282844 EUDAMED08591285281885 EUDAMED08591285085292 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, 4+K 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 |
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Manufacturer
- Manufacturer
- MAXIS a.s.
- EUDAMED SRN
- CZ-MF-000000989
Sources (3)
- EUDAMED 72c320e7-5cd8-4bbf-8c38-d75c6d117c16 61 fields · synced Oct 7, 2026
- EUDAMED 945ce550-2f16-4d39-a6b4-7abb1c5e57bc 61 fields · synced May 16, 2026
- EUDAMED 760f5249-c544-408a-8aae-a5f7058f2503 61 fields · synced May 17, 2026