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.

VENOFLEX MICRO — 862 UDI-DI variants, MDR (Thuasne Deutschland GmbH)

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

VENOFLEX MICRO

4035459DE1406B3Y

862 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: Thuasne Deutschland GmbH

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: 4035459DE1406B3Y
Device name: VENOFLEX MICRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Thuasne Deutschland GmbH
SRN: DE-MF-000006210
Country: Germany
Email: ra@thuasne.de

Variants by status

UDI-DI variants

862 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

basicUdiUlid01KCTZYYHQ171KDA6D355JANZG

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

30023E2140151104035459288873
30023E2220252204035459289931
30023E2120151304035459288415
30023E2150151204035459289122
30023H2140302304035459291927
30023E2120152304035459288446
30023E2240152304035459290364
30025B2060151204035459294690
30023E2120301304035459288538
30023H2140252104035459291842
30027B2050152204035459295048
30023E2250151304035459290579
30023H2210032304035459292467
30023E2130252304035459288743
30023H2150032104035459291965
30023H2110302304035459291200
30021B2040152304035459287203
30023H2240252104035459293280
30023H2210252304035459292580
30023E2250032104035459290524
30023E2130301304035459288774
30023H2210151104035459292474
30027B2020301204035459287890
30023H2220151204035459292726
30023H2140152304035459291804

2 3 4 5 6