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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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VENOFLEX MICRO — 864 UDI-DI variants, MDR (Thuasne Deutschland GmbH)

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

VENOFLEX MICRO

4035459DE1406A3W

864 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

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UDI-DI variants

864 UDI-DI variants

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Applied filters

basicUdiUlid01KEF2GWM19R391GV2M2CJ6Y3S

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

30021A2040032304035459305303
30025A2010032204035459311533
30023G2120302304035459309103
30023G2250251304035459311175
30025A2060301204035459312431
30023D2150301304035459306911
30025A2020151304035459311724
30023G2210302304035459310307
30023D2160252204035459307116
30023D2260302204035459308618
30023D2220301304035459307635
30025A2050152304035459312226
30023G2150302204035459309813
30023G2230032304035459310604
30023G2120032104035459308908
30023D2230302104035459307888
30023G2230301304035459310758
30023D2150032304035459306768
30021A2040251304035459305365
30023D2130032304035459306287
30021A2020301104035459305075
30021A2010302104035459304931
30023G2110301304035459308830
30023D2120252204035459306157
30023D2160302304035459307185

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035459DE1406A3W
Device name: VENOFLEX MICRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status