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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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Barelle — 7 UDI-DI variants, MDR (CFS ITALIA SRL)

MD Atlas
CFS ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

Barelle

805803257CFSBARAA

7 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: CFS ITALIA SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805803257CFSBARAA
Device name: —
Device model: Barelle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: CFS ITALIA SRL
SRN: IT-MF-000045084
Country: Italy
Email: comitalia@cfsitalia.com
Phone: +390422397333

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01JRZ28QBESAJKT0B1KVGS28RF

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

LO503-11108058032573384
LO503-11808058032573438
LO503-12008058032573445
LO503-21108058032573391
LO503-21208058032573407
LO503-22108058032573414
LO503-22208058032573421