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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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ANI Sensor V1 PLUS — 2 UDI-DI variants, MDR

MD Atlas
MDoloris Medical Systems SAS

Data from EUDAMED, last updated May 19, 2026

ANI Sensor V1 PLUS

376023246ANI-SENSV1PLUSEH

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: MDoloris Medical Systems SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376023246ANI-SENSV1PLUSEH
Device name: ANI Sensor V1 PLUS
Device model: ANI Sensor V1 PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: MDoloris Medical Systems SAS
SRN: FR-MF-000000421
Country: France
Email: jm.jeromemartinez@gmail.com
Phone: +33 6 71 73 16 52

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FTTD8JTAE1NRX30CZMA1G682

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

ANI Sensor V1 PLUS03760232460436
MDoloris Medical Systems03760232460313