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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 Gas — 12 UDI-DI variants, MDR (Lomar srl)

MD Atlas
Lomar srl

Data from EUDAMED, last updated May 31, 2026

Lomar Medical Testaletto Gas

805957160002FV

12 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Lomar srl

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 805957160002FV
Device name: Lomar Medical Testaletto Gas
Device model: Lomar Medical Testaletto Gas
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 10, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JRFNFTYK70KYEW2RQG25H7XT

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

Combi Gas 80595716000506
Combi Gas B80595716000438
Combi Gas P80595716000674
Intensiva P80595716001282
Intensiva SC80595716001350
Intensiva SDC80595716001596
Intensiva SDI80595716001664
Intensiva SI80595716001428
Start Gas80595716000810
Start V80595716000988
Verti 180595716001046
Verti 280595716001114