Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Kompresní punčochy MICRO III.KT -… — 165 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO III.KT - Stehenní punčocha s upínáním v pase pravá

8591285UPPM3BP

165 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285UPPM3BP
Device name: Kompresní punčochy MICRO III.KT - Stehenní punčocha s upínáním v pase pravá
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

165 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KPT6YPHT8RT1YCK2SFPBRCG6

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

859128596009408591285960094
859128596008708591285960087
859128596006308591285960063
859128596007008591285960070
859128508277208591285082772
859128590818808591285908188
859128590820108591285908201
859128590816408591285908164
859128590817108591285908171
859128508278908591285082789
859128596014808591285960148
859128596013108591285960131
859128596011708591285960117
859128596012408591285960124
859128508279608591285082796
859128590828708591285908287
859128590830008591285908300
859128590826308591285908263
859128590827008591285908270
859128508280208591285082802
859128596019308591285960193
859128596018608591285960186
859128596016208591285960162
859128596017908591285960179
859128508281908591285082819

1 2 3 4 5