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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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cuffie e copricapo — 5 UDI-DI variants, MDR

MD Atlas
3 M.C. Società per azioni

Data from EUDAMED, last updated May 30, 2026

cuffie e copricapo

805430128T0207VD

5 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: 3 M.C. Società per azioni

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805430128T0207VD
Device name: cuffie e copricapo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: 3 M.C. Società per azioni
SRN: IT-MF-000022649
Country: Italy
Email: belviso@tremc.eu
Phone: +39804552385

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJ2Z71FH69QFJ6EJGY63GPWW

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

d/101280543012800696
D/1013/180543012807176
D/101380543012807008
224080543012810978
223980543012811036