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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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K Myo — 2 UDI-DI variants, MDR (KINVENT Biomecanique)

MD Atlas
KINVENT Biomecanique

Data from EUDAMED, last updated May 19, 2026

K Myo

3770011995KMyo95

2 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: KINVENT Biomecanique

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770011995KMyo95
Device name: K Myo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: KINVENT Biomecanique
SRN: FR-MF-000031884
Country: France
Email: info@k-invent.com
Phone: +33467130033

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HG8CWMTHR4526R0288KYFPHT

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

MP.10.02.FN03770011995707
MP.10.03.FN03770011995875