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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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EURO 9702 — 2 UDI-DI variants, MDR (HOME MEDICAL SERVICE H.M.S.)

MD Atlas
HOME MEDICAL SERVICE H.M.S.

Data from EUDAMED, last updated May 19, 2026

EURO 9702

361580EURO950077

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: HOME MEDICAL SERVICE H.M.S.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 361580EURO950077
Device name: EURO 9702
Device model: EURO 9702
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: HOME MEDICAL SERVICE H.M.S.
SRN: FR-MF-000028528
Country: France
Email: christian.jude@hms-vilgo.com
Phone: +33320848150

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JM1XT031HT5PNRFV5CBJ0ABE

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

EURO 970203615800006243
EURO 9702-1M 03615800006250