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.

Rukavice vyšetřovací — 120 UDI-DI variants, MDR

MD Atlas
STERIWUND spol. s r.o.

Data from EUDAMED, last updated May 23, 2026

Rukavice vyšetřovací

85951541005VE

120 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: STERIWUND spol. s r.o.

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: 85951541005VE
Device name: Rukavice vyšetřovací
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: STERIWUND spol. s r.o.
SRN: CZ-MF-000036963
Country: Czechia
Email: steriwund@steriwund.cz
Phone: +420 733 110 862

Variants by status

UDI-DI variants

120 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

basicUdiUlid01KMJ2TKYQ1DN0Z670SXA4XVWM

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

1164/10008595154112485
1165/10008595154112669
1165/1008595154112638
1164/2008595154112461
1102/10008595154112607
1102/1008595154112577
1165/2008595154112645
1101/208595154112492
1102/2008595154112584
1164/208595154112430
1165/608595154112621
1101/2008595154112522
1101/608595154112508
1165/208595154112614
1102/5008595154112591
1165/5008595154112652
1102/608595154112560
1164/1008595154112454
1102/208595154112553
1101/1008595154112515

1 2 3 4 5