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III.S MICRO, AG-HB PRAVÁ, vel.2N, světlá

EUDAMED

Class I (EU MDR)

Ref 8591285907365Ref 8591285897963Ref 8591285908164

by MAXIS a.s.

Identity

Trade Name
III.S MICRO,AG-HB PRAVÁ,vel.2N,světlá EUDAMED
III.S MICRO,AG,vel.2N,světlá EUDAMED
III. MICRO,AG-HB PRAVÁ,vel.2N,světlá EUDAMED
Device Name
Kompresní punčochy MICRO III.KT - Stehenní punčocha s upínáním v pase pravá EUDAMED
Kompresní punčochy MICRO III.KT - Stehenní punčocha EUDAMED
Model / Reference
8591285907365 EUDAMED
8591285897963 EUDAMED
8591285908164 EUDAMED

Identifiers

Primary DI / UDI-DI
08591285907365 EUDAMED
08591285897963 EUDAMED
08591285908164 EUDAMED
Basic UDI-DI
8591285UPPM3BP EUDAMED
8591285AGM36F 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

III.S MICRO, AG-HB PRAVÁ, vel.2N, 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 (3)

  • EUDAMED 8f99948f-1e8b-40ab-8d8b-5d35d991eafd 61 fields · synced Jul 9, 2026
  • EUDAMED 8f2e5d69-ddba-4c82-8cdc-2a9ab94dc534 61 fields · synced May 17, 2026
  • EUDAMED 90fb011e-88c9-4792-a738-0d61e804f080 61 fields · synced May 18, 2026