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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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Lomar Medical Testaletto — 7 UDI-DI variants, MDR (Lomar srl)

MD Atlas
Lomar srl

Data from EUDAMED, last updated May 30, 2026

Lomar Medical Testaletto

805957160001FT

7 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: Lomar srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805957160001FT
Device name: Lomar Medical Testaletto
Device model: Lomar Medical Testaletto
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Lomar srl
SRN: IT-MF-000013947
Country: Italy
Email: medicale@lomar.it
Phone: 0302680572

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GFX6Z6A44KPKD0YKYPK0PK8R

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

Aura compact80595716002036
Lumina80595716001978
Start80595716000742
Start mini80595716001800
Style80595716000124
Style L80595716000360
Style P80595716000292