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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 MICRO II.KT -… — 160 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO II.KT - Stehenní punčocha s upínáním v pase levá

8591285UPLM2AZ

160 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: 8591285UPLM2AZ
Device name: Kompresní punčochy MICRO II.KT - Stehenní punčocha s upínáním v pase levá
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

UDI-DI variants

160 UDI-DI variants

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Applied filters

basicUdiUlid01KPSXHKDFT3FX82S5H20H2VP1

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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859128524107008591285241070
859128524105608591285241056
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859128506874508591285068745
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859128524218308591285242183
859128524217608591285242176
859128524215208591285242152
859128524216908591285242169
859128506876908591285068769
859128524308108591285243081
859128524307408591285243074
859128524305008591285243050
859128524306708591285243067

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