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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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MTR, MTR_ANTIDEC — 6 UDI-DI variants, MDR (Malvestio Spa)

MD Atlas
Malvestio Spa

Data from EUDAMED, last updated May 31, 2026

MTR, MTR_ANTIDEC

805830260MBSL

6 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805830260MBSL
Device name: MTR, MTR_ANTIDEC
Device model: 304700, 304700A, 304700XL, 304700XLA, 304720, 304740
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KSFDCTSGQCQXMN95G6BBSFY0

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

30470008058302602868
304700A08058302602882
304700XL08058302602875
304700XLA08058302602899
30474008058302602912
30472008058302602905