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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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IVS3 — 7 UDI-DI variants, MDR (DESSINTEY)

MD Atlas
DESSINTEY

Data from EUDAMED, last updated May 19, 2026

IVS3

3770024593IVS33B

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: DESSINTEY

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770024593IVS33B
Device name: IVS3
Device model: IVS3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: DESSINTEY
SRN: FR-MF-000009697
Country: France
Email: qualite@dessintey.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01G7EQBFXGR1PDPGQSAHBYY7WB

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

IVS3 - ESP03770024593082
IVS3 - NORDIC03770024593129
IVS3 - BEL03770024593075
IVS3 - EUR03770024593266
IVS303770024593006
IVS3 (with EU cord and QWERTZ-DE Keyboard)03770024593112
IVS3 - ITA03770024593037