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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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Sensori — 6 UDI-DI variants, MDR (BIONEN SRL)

MD Atlas
BIONEN SRL

Data from EUDAMED, last updated May 31, 2026

Sensori

803331512SENS0025FP

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: BIONEN SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803331512SENS0025FP
Device name: Sensori
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIONEN SRL
SRN: IT-MF-000018461
Country: Italy
Email: info@bionen.it
Phone: 0554265945

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KN469X5VW0CVNA6G1T3H70ND

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

0043.00108033315124422
0018.06008033315124125
0018.06108033315124132
0018.07108033315124149
0018.07208033315124569
0018.10308033315124156