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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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Letti LYTUS tre sezioni — 4 UDI-DI variants, MDR (MORETTI SPA)

MD Atlas
MORETTI SPA

Data from EUDAMED, last updated May 30, 2026

Letti LYTUS tre sezioni

805287964202301Q9

4 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: MORETTI SPA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805287964202301Q9
Device name: Letti LYTUS tre sezioni
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: MORETTI SPA
SRN: IT-MF-000005980
Country: Italy
Email: info@morettispa.com
Phone: +39055962111

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HAXXNZRAQK2HFKRBA3B0PKPY

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

MI310B08052879646355
MI321B08052879646072
MI320B08052879646034
MI311B08052879646393