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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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SOLDEX — 4 UDI-DI variants, MDR (LIDERMED S.A.)

MD Atlas
LIDERMED S.A.

Data from EUDAMED, last updated May 23, 2026

SOLDEX

18426716SLDEX01S2

4 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: LIDERMED S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 18426716SLDEX01S2
Device name: SOLDEX
Device model: INMOVILIZADOR DE CLAVICULA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: LIDERMED S.A.
SRN: ES-MF-000004664
Country: Spain
Email: mario@lidermed.com
Phone: 663133901

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KJSCZKPKN9FXNTQ0QGJVH24N

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

004060708426716406073
004060608426716406066
004060508426716406059
004060408426716406042