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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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Turbo DECCS — 2 UDI-DI variants, MDR (MEDIVAC S.R.L. SOCIETA' BENEFIT)

MD Atlas
MEDIVAC S.R.L. SOCIETA' BENEFIT

Data from EUDAMED, last updated May 30, 2026

Turbo DECCS

805368965MT23JV

2 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: MEDIVAC S.R.L. SOCIETA' BENEFIT

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Device characteristics

Active deviceHuman tissues / cells

Identity & classification

Basic UDI-DI: 805368965MT23JV
Device name: —
Device model: Turbo DECCS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: MEDIVAC S.R.L. SOCIETA' BENEFIT
SRN: IT-MF-000030012
Country: Italy
Email: info@medivac.it
Phone: +39 05211815968

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GPAX9ER5SSSW61D7X6ER6GQ0

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

TD1408053689650006
MT2308053689650013