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II. BRILLANT, AG, vel.2+K, krajka, světlá
EUDAMEDClass I (EU MDR)
Ref 8591285828417Ref 8591285826017
by MAXIS a.s.
Identity
- Trade Name
- II. BRILLANT,AG,vel.2+K,krajka,světlá EUDAMEDII.S BRILLANT,AG,vel.2+K,krajka,světlá EUDAMED
- Device Name
- Kompresní punčochy BRILLANT II.KT - Stehenní punčocha s krajkou EUDAMED
- Model / Reference
- 8591285828417 EUDAMED8591285826017 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08591285828417 EUDAMED08591285826017 EUDAMED
- Basic UDI-DI
- 8591285AGKB2YV 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. BRILLANT, AG, vel.2+K, krajka, světlá 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
- MEDI — MEDI MANUFACTURING, INC. · Class II
- JOBST Relief — BSN MEDICAL, INC. · Class II
- VenoTrain micro — Bauerfeind GmbH & Co. · Class II
- Essential CLASSICAL — SIGVARIS 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 | 8591285AGKB2YV | Class I | Active |
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Manufacturer
- Manufacturer
- MAXIS a.s.
- EUDAMED SRN
- CZ-MF-000000989
Sources (2)
- EUDAMED 4c35ed4b-fcbc-4564-ab15-eabaeca15844 61 fields · synced Oct 6, 2026
- EUDAMED 1984be11-d907-4452-ab68-3b096364fb19 61 fields · synced May 19, 2026