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.

Návleky na horní končetiny MICRO II.KT… — 63 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Návleky na horní končetiny MICRO II.KT - Pažní návlek s rukavicí s úchytem

8591285PNR2B8

63 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: 8591285PNR2B8
Device name: Návleky na horní končetiny MICRO II.KT - Pažní návlek s rukavicí s úchytem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 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

63 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

basicUdiUlid01KQ6ZGE4BG4P7MF7HZYF81NBE

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

859128512010808591285120108
859128512022108591285120221
859128512021408591285120214
859128512034408591285120344
859128512033708591285120337
859128512046708591285120467
859128512045008591285120450
859128512058008591285120580
859128512057308591285120573
859128512005408591285120054
859128512017708591285120177
859128512009208591285120092
859128512070208591285120702
859128512069608591285120696
859128549761308591285497613
859128512545508591285125455
859128512544808591285125448
859128549758308591285497583
859128549774308591285497743
859128549775008591285497750
859128549776708591285497767
859128549777408591285497774
859128511076508591285110765
859128511075808591285110758
859128506056508591285060565

1 2 3