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 -… — 147 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO III.KT - Polostehenní punčocha s krajkou

8591285AFKM3ZR

147 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: 8591285AFKM3ZR
Device name: Kompresní punčochy MICRO III.KT - Polostehenní punčocha s krajkou
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

147 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

basicUdiUlid01KPT6M41HN5R3EF7WKB6S3PDN

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

859128593348708591285933487
859128593346308591285933463
859128593347008591285933470
859128508051808591285080518
859128593889508591285938895
859128593888808591285938888
859128593886408591285938864
859128593887108591285938871
859128508056308591285080563
859128593354808591285933548
859128593353108591285933531
859128593351708591285933517
859128593352408591285933524
859128508057008591285080570
859128593894908591285938949
859128593893208591285938932
859128593891808591285938918
859128593892508591285938925
859128508062408591285080624
859128593359308591285933593
859128593358608591285933586
859128593356208591285933562
859128593357908591285933579
859128508063108591285080631
859128593899408591285938994

1 2 3 4 5