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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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Solsius SelfCare Insole — 12 UDI-DI variants, MDR (Solsius SAS)

MD Atlas
Solsius SAS

Data from EUDAMED, last updated May 19, 2026

Solsius SelfCare Insole

3760430740001VP

12 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: Solsius SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3760430740001VP
Device name: Solsius SelfCare Insole
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Solsius SAS
SRN: FR-MF-000041700
Country: France
Email: admin@solsius.fr

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01JZHZ35T0EYZSEBZ5QJGD1ZJP

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

INSOLE-T2-R03760430740095
INSOLE-T4-R03760430740019
INSOLE-T1-L03760430740118
INSOLE-T3-L03760430740057
INSOLE-T2-L03760430740088
INSOLE-T403760430740026
INSOLE-T203760430740101
INSOLE-T4-L03760430740002
INSOLE-T3-R03760430740064
INSOLE-T1-R03760430740125
INSOLE-T303760430740071
INSOLE-T103760430740132