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… — 25 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 lemem + rukavice

8591285PNSL29U

25 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: 8591285PNSL29U
Device name: Návleky na horní končetiny MICRO II.KT - Pažní návlek s lemem + rukavice
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

25 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

basicUdiUlid01KQ6S7NTT53GDGFN0VFQ9ZJW2

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

859128510602708591285106027
859128510570908591285105709
859128510604108591285106041
859128510572308591285105723
859128510606508591285106065
859128511109008591285111090
859128511108308591285111083
859128511411408591285114114
859128511410708591285114107
859128511423708591285114237
859128511422008591285114220
859128514578108591285145781
859128514577408591285145774
859128514580408591285145804
859128514579808591285145798
859128514582808591285145828
859128514581108591285145811
859128514584208591285145842
859128514583508591285145835
859128514586608591285145866
859128514585908591285145859
859128514588008591285145880
859128514587308591285145873
859128514590308591285145903
859128514589708591285145897