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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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Fixation devices — 7 UDI-DI variants, MDR (MedEnvision bv)

MD Atlas
MedEnvision bv

Data from EUDAMED, last updated May 23, 2026

Fixation devices

5430001422MEFDLH

7 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: MedEnvision bv

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430001422MEFDLH
Device name: Fixation devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: MedEnvision bv
SRN: BE-MF-000000329
Country: Belgium
Email: info@medenvision.com
Phone: +3216237527

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01G2A2QQZ7CEZMYVVY1T31K6Z0

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

ME-FD500005430001422146
ME-FD2000L05430001422108
ME-FD3000S05430001422139
ME-FD1000S05430001422092
ME-FD2000S05430001422115
ME-FD3000L05430001422122
ME-FD1000L05430001422085