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II., PROMAX, AG, 3K protiskluz.lem, tělová
EUDAMEDClass I (EU MDR)
Ref 8591285281847Ref 8591285084790Ref 8591285085117
by MAXIS a.s.
Identity
- Trade Name
- II.,PROMAX,AG,3K protiskluz.lem,tělová EUDAMEDII.,S,PROMAX,AG,3K protiskluz.lem,tělová EUDAMED
- Device Name
- Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením EUDAMED
- Model / Reference
- 8591285281847 EUDAMED8591285084790 EUDAMED8591285085117 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285281847 EUDAMED08591285084790 EUDAMED08591285085117 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, 3K protiskluz.lem, tělová by MAXIS a.s. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 (3)
- EUDAMED d445b6d4-8062-4823-9277-b18ab8e5e309 61 fields · synced Jul 27, 2026
- EUDAMED 1f348d66-529b-4278-8c89-ebdeb2fb77a0 61 fields · synced May 16, 2026
- EUDAMED 185991d4-dac8-4136-b4e6-c46f6ab19ee0 61 fields · synced May 18, 2026