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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

859128505775608591285057756
859128581483008591285814830
859128509702808591285097028
859128581481608591285814816
859128581482308591285814823
859128505776308591285057763
859128581488508591285814885
859128509703508591285097035
859128581486108591285814861
859128581487808591285814878
859128505777008591285057770
859128581493908591285814939
859128581491508591285814915
859128581492208591285814922
859128505778708591285057787
859128581498408591285814984
859128509705908591285097059
859128581496008591285814960
859128581497708591285814977
859128505779408591285057794
859128581503508591285815035
859128581501108591285815011
859128581502808591285815028
859128505780008591285057800
859128581508008591285815080

2 3 4 5 6

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