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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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Materassi gonfiabili. — 9 UDI-DI variants, MDR (VASSILLI S.R.L.)

MD Atlas
VASSILLI S.R.L.

Data from EUDAMED, last updated May 30, 2026

Materassi gonfiabili.

805527193MatCom001TB

9 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

Active device

Identity & classification

Basic UDI-DI: 805527193MatCom001TB
Device name: Materassi gonfiabili.
Device model: MatCom001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2026

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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJS8KVMC0TYNSHCJ4GTZK63S

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

20.2008055271933412
20.20/12008055271935133
20.20A08055271934976
20.20DH2108055271933702
20.20DH21/12008055271933771
20.20F08055271933474
20.2208055271933429
20.22/1308055271933481
20.22A08055271935683