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II., PROMAX, AD, 3K, tělová
EUDAMEDClass I (EU MDR)
Ref 8591285084479
by MAXIS a.s.
Identity
- Trade Name
- II.,PROMAX,AD,3K,tělová EUDAMED
- Device Name
- Kompresní punčochy PROMAX Standard II.KT - Lýtková punčocha EUDAMED
- Model / Reference
- 8591285084479 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285084479 EUDAMED
- Basic UDI-DI
- 8591285ADP267 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, AD, 3K, 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.
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- MEDI — MEDI MANUFACTURING, INC. · Class II
- JOBST Relief — BSN MEDICAL, INC. · Class II
- VenoTrain micro — Bauerfeind GmbH & Co. · Class II
- VenoTrain soft, AG, Top band silicone micro dots, Ccl2, open toe, L Plus short, Cream — Bauerfeind AG · Class I
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 | 8591285ADP267 | Class I | Active |
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Manufacturer
- Manufacturer
- MAXIS a.s.
- EUDAMED SRN
- CZ-MF-000000989
Sources (1)
- EUDAMED a0c86fe7-dc3f-4130-8a3f-9b915f237770 61 fields · synced Jun 19, 2026