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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 I.KT -… — 181 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO I.KT - Punčochové kalhoty

8591285ATM18C

181 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: 8591285ATM18C
Device name: Kompresní punčochy MICRO I.KT - Punčochové kalhoty
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 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

181 UDI-DI variants

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Applied filters

basicUdiUlid01KPQ736CXBP26GPMGRVVNV3GS

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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859128587215108591285872151
859128587211308591285872113
859128587212008591285872120
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859128587222908591285872229
859128514542208591285145422
859128507824908591285078249
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859128587230408591285872304
859128587226708591285872267
859128587227408591285872274
859128507825608591285078256
859128514721108591285147211

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