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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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LM 3060 W — 8 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

LM 3060 W

361580HARMONIETWICEHP

8 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: 361580HARMONIETWICEHP
Device name: LM 3060 W
Device model: HARMONIE TWICE
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01JM29S1P1HQ8DVCTSM960250Q

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

LM 3060 W03615800047710
LM 3062 W03615800047734
LM 3064 W03615800047758
LM 3066 W03615800047772
LM 3260 W03615800047727
LM 3262 W03615800047741
LM 3264 W03615800047765
LM 3266 W03615800047789