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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 manuali. — 10 UDI-DI variants, MDR (VASSILLI S.R.L.)

MD Atlas
VASSILLI S.R.L.

Data from EUDAMED, last updated May 30, 2026

Letti manuali.

805527193LetMan001UF

10 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: VASSILLI S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805527193LetMan001UF
Device name: Letti manuali.
Device model: LetMan001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: VASSILLI S.R.L.
SRN: IT-MF-000033141
Country: Italy
Email: info@vassilli.it

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JPQ9GRWNM5A8SFHTK7HQGBWZ

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

10.62E08055271932163
10.62EP08055271932170
10.62EPR08055271932187
10.62ET08055271932194
10.64E08055271931906
10.64E/12008055271931890
10.64EP08055271932200
10.64EPR08055271932217
10.64ET08055271931876
10.64ET/12008055271932224