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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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SOLUKAT — 5 UDI-DI variants, MDR (GERGONNE INDUSTRIE)

MD Atlas
GERGONNE INDUSTRIE

Data from EUDAMED, last updated May 19, 2026

SOLUKAT

0370148760199904038B

5 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: GERGONNE INDUSTRIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0370148760199904038B
Device name: SOLUKAT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: GERGONNE INDUSTRIE
SRN: FR-MF-000003647
Country: France
Email: contact.fr@gergonne.com
Phone: +33 4 74 73 39 01

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HY38SCTH8E2X60YKJ1S3E1NA

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

PADS100003701487600048
PADS100003701487600260
S1W03701487600291
PADS1000SI03701487600086
PADS1000SI03701487600277