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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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MAHI by EXONEO — 20 UDI-DI variants, MDR (EXONEO)

MD Atlas
EXONEO

Data from EUDAMED, last updated May 19, 2026

MAHI by EXONEO

37700158050398

20 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: EXONEO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37700158050398
Device name: MAHI by EXONEO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: EXONEO
SRN: FR-MF-000003061
Country: France
Email: contact@exoneo.eu

Variants by status

UDI-DI variants

20 UDI-DI variants

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Applied filters

basicUdiUlid01GZGE42XBA9EF4A4WFWE3W78J

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

03CDC2-P637700158055696
03CDC1-P237700158053784
03CGC2-P337700158054538
03CDC2-P537700158054606
03CGC1-P537700158054088
03CGC2-P237700158054392
03CGC1-P637700158054224
03CDC1-P637700158054910
03CDC1-P337700158053852
03CGC2-P637700158054460
03CDC1-P437700158053920
03CGC2-P537700158055450
03CDC1-P537700158055214
03CDC2-P337700158055528
03CGC1-P237700158055078
03CGC1-P437700158055382
03CDC2-P437700158054842
03CGC1-P337700158054774
03CDC2-P237700158055146
03CGC2-P437700158054156