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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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RACCORDO DI CONNESSIONE PER TUBO — 4 UDI-DI variants, MDR

MD Atlas
F.LLI MARCHESI SRL

Data from EUDAMED, last updated May 30, 2026

RACCORDO DI CONNESSIONE PER TUBO

805681472RACCG6

4 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: F.LLI MARCHESI SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805681472RACCG6
Device name: RACCORDO DI CONNESSIONE PER TUBO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: F.LLI MARCHESI SRL
SRN: IT-MF-000040181
Country: Italy
Email: valerio.marchesi@fratellimarchesi.it

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JNRFEPBAHHB3YCSDTNPP01BD

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

PL00207SA0008056814720179
PL00217SF0008056814720094
PL00217CCSF08056814720087
PL00207SF0008056814720162