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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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Knee high (open foot) — 10 UDI-DI variants, MDR (Medtex Swiss Ltd)

MD Atlas
Medtex Swiss Ltd

Data from EUDAMED, last updated May 31, 2026

Knee high (open foot)

380023248B16022CH

10 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: 380023248B16022CH
Device name: Knee high (open foot)
Device model: 1602
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KRBHVCDAF047GFTK45D55KYC

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

Knee high (open foot)03800232485357
Knee high (open foot)03800232485364
Knee high (open foot)03800232485319
Knee high (open foot)03800232485326
Knee high (open foot)03800232485395
Knee high (open foot)03800232485340
Knee high (open foot)03800232485371
Knee high (open foot)03800232485333
Knee high (open foot)03800232485388
160203800232485302