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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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KinTracK — 2 UDI-DI variants, MDR (EKINNOX)

MD Atlas
EKINNOX

Data from EUDAMED, last updated May 19, 2026

KinTracK

3770017707019V

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: EKINNOX

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770017707019V
Device name: KinTracK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: EKINNOX
SRN: FR-MF-000000917
Country: France
Email: baptiste.fosty@ekinnox.com
Phone: +33623602440

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JKGCJV0A3JF6TE3ZZF7XB4S7

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

KinTracK version 303770017707014
KinTracK version 203770017707007