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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 II.KT -… — 277 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy BRILLANT II.KT - Stehenní punčocha s lemem

8591285AGLB2Z2

277 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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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285AGLB2Z2
Device name: Kompresní punčochy BRILLANT II.KT - Stehenní punčocha s lemem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 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

UDI-DI variants

277 UDI-DI variants

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Applied filters

basicUdiUlid01KPWEGKV6WWE8XEBBM2K99R55

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

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859128582498308591285824983
859128509810008591285098100
859128582496908591285824969
859128582497608591285824976
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859128582517108591285825171
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859128582528708591285825287
859128582526308591285825263
859128582527008591285825270
859128505909508591285059095
859128583028108591285830281
859128583026708591285830267

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