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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Kompresní punčochy BRILLANT I.KT -… — 135 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy BRILLANT I.KT - Punčochové kalhoty

8591285ATB17B

135 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MAXIS a.s.

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UDI-DI variants

135 UDI-DI variants

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Applied filters

basicUdiUlid01KPTHZQHGPJD8PCSEBPC45X3Y

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

859128505751008591285057510
859128581523308591285815233
859128581521908591285815219
859128581522608591285815226
859128505752708591285057527
859128581528808591285815288
859128581526408591285815264
859128581527108591285815271
859128505753408591285057534
859128581533208591285815332
859128509680908591285096809
859128581531808591285815318
859128581532508591285815325
859128505754108591285057541
859128581538708591285815387
859128581536308591285815363
859128581537008591285815370
859128505755808591285057558
859128581543108591285815431
859128581541708591285815417
859128581542408591285815424
859128505756508591285057565
859128581548608591285815486
859128581546208591285815462
859128581547908591285815479

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285ATB17B
Device name: Kompresní punčochy BRILLANT I.KT - Punčochové kalhoty
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: MAXIS a.s.
SRN: CZ-MF-000000989
Country: Czechia
Email: info@maxis-medica.com
Phone: +420571633510

Variants by status