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I. BRILLANT, AD, vel.3K, světlá

EUDAMED

Class I (EU MDR)

Ref 8591285801014Ref 8591285800215

by MAXIS a.s.

Identity

Trade Name
I. BRILLANT,AD,vel.3K,světlá EUDAMED
I.S BRILLANT,AD,vel.3K,světlá EUDAMED
Device Name
Kompresní punčochy BRILLANT I.KT - Lýtková punčocha EUDAMED
Model / Reference
8591285801014 EUDAMED
8591285800215 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285801014 EUDAMED
08591285800215 EUDAMED
Basic UDI-DI
8591285ADB14T 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

I. BRILLANT, AD, vel.3K, 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.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
MAXIS a.s.
EUDAMED SRN
CZ-MF-000000989

Sources (2)

  • EUDAMED 21f6c14c-7a25-4664-a1b6-302be27c273b 61 fields · synced Jul 26, 2026
  • EUDAMED a3d38e2f-0ad3-4879-890b-9e4855e8e936 61 fields · synced May 18, 2026