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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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Derotation boot — 2 UDI-DI variants, MDR (Medtex Swiss Ltd)

MD Atlas
Medtex Swiss Ltd

Data from EUDAMED, last updated May 23, 2026

Derotation boot

3800232482301RQ

2 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: Medtex Swiss Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3800232482301RQ
Device name: Derotation boot
Device model: 7040
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Medtex Swiss Ltd
SRN: BG-MF-000023453
Country: Bulgaria
Email: medtex.swiss@gmail.com
Phone: +359886697729

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G390MY7V2DJFGTJXASZ8GRXM

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

MedTextile03800232482301
MedTextile03800232484558