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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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myDiabby Healthcare — 5 UDI-DI variants, MDR (MDHC SAS)

MD Atlas
MDHC SAS

Data from EUDAMED, last updated May 19, 2026

myDiabby Healthcare

3770026228MYDIABBYXQ

5 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: MDHC SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770026228MYDIABBYXQ
Device name: myDiabby Healthcare
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: Dec 19, 2023

Manufacturer & authorised representative

Manufacturer

Name: MDHC SAS
SRN: FR-MF-000023668
Country: France
Email: hello@mydiabby.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HJ0KNWC637RX3PN61VPEX7D5

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

myDiabby Healthcare [BE]03770026228029
myDiabby Healthcare03770026228043
myDiabby Healthcare [EN]03770026228012
myDiabby Healthcare [FR]03770026228005
myDiabby Healthcare03770026228036