Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

DESIDIA 2.0, SICURA 2.0, SYESTA 2.0,… — 14 UDI-DI variants, MDR

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 30, 2026

DESIDIA 2.0, SICURA 2.0, SYESTA 2.0, VALEA 2.0

805830260POLTRELAXSG

14 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: Malvestio Spa

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805830260POLTRELAXSG
Device name: DESIDIA 2.0, SICURA 2.0, SYESTA 2.0, VALEA 2.0
Device model: 364501, 364511, 364521, 364611, 364621, 364751, 364851, 364816, 364826, 364701, 364711, 364721, 364811, 364821
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Malvestio Spa
SRN: IT-MF-000013307
Country: Italy
Email: info@malvestio.it
Phone: +39 049 9299511

Variants by status

UDI-DI variants

14 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSJ077DGWH0NQ93RZ3B0GPB1

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

36461108058302602073
36462108058302602080
36450108058302602042
36452108058302602066
36451108058302602059
36485108058302602172
36475108058302602127
36482608058302602165
36481608058302602141
36471108058302602103
36482108058302602158
36470108058302602097
36472108058302602110
36481108058302602134