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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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Kinevia Duo — 2 UDI-DI variants, MDR (Kinetec SAS)

MD Atlas
Kinetec SAS

Data from EUDAMED, last updated May 19, 2026

Kinevia Duo

376024624APTRAINERGH

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Kinetec SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376024624APTRAINERGH
Device name: Kinevia Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Kinetec SAS
SRN: FR-MF-000000364
Country: France
Email: contact@kinetec.fr

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KM03S34AX8HBEPQT0EBZXRCG

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

Kinevia - KINETEC SAS03760246246996
Kinevia Duo - KINETEC SAS03760246246989