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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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VenoTrain cocoon — 128 UDI-DI variants, MDR (Bauerfeind AG)

MD Atlas
Bauerfeind AG

Data from EUDAMED, last updated May 23, 2026

VenoTrain cocoon

4046445COC00000000FB

128 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: Bauerfeind AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046445COC00000000FB
Device name: VenoTrain cocoon
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bauerfeind AG
SRN: DE-MF-000007543
Country: Germany
Email: regulatory.affairs@bauerfeind.com
Phone: +49 36628 66 1000

Variants by status

UDI-DI variants

128 UDI-DI variants

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Applied filters

basicUdiUlid01KKKGMPVSE8ZN632N6FB259FZ

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

VenoTrain cocoon, AD, Ccl 2, closed toe, foot short, XL Normal short, Black04057532093860
VenoTrain cocoon, AD, Ccl 2, closed toe, foot short, XL Plus long, Black04057532094287
VenoTrain cocoon, AD, Ccl 2, closed toe, foot short, XL Plus short, Black04057532094249

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