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 PROMAX Standard… — 192 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením

8591285AGLP22F

192 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: 8591285AGLP22F
Device name: Kompresní punčochy PROMAX Standard II.KT - Stehenní punčocha s neklouzavým zakončením
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 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

192 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

basicUdiUlid01KPYXVHSQ4HKZDM6TKHAR2RRE

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

859128528209708591285282097
859128508491208591285084912
859128528208008591285282080
859128528211008591285282110
859128508492908591285084929
859128528210308591285282103
859128528177908591285281779
859128528176208591285281762
859128508475208591285084752
859128528179308591285281793
859128528178608591285281786
859128508476908591285084769
859128528213408591285282134
859128528212708591285282127
859128508493608591285084936
859128528215808591285282158
859128508494308591285084943
859128528214108591285282141
859128528181608591285281816
859128508477608591285084776
859128528180908591285281809
859128528183008591285281830
859128508478308591285084783
859128528182308591285281823
859128528217208591285282172

1 2 3 4 5