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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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FARMASAFE@ — 4 UDI-DI variants, MDR (Dedalus Italia SpA)

MD Atlas
Dedalus Italia SpA

Data from EUDAMED, last updated May 30, 2026

FARMASAFE@

805572803FARMASAFEDG

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Dedalus Italia SpA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805572803FARMASAFEDG
Device name: FARMASAFE@
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Dedalus Italia SpA
SRN: IT-MF-000009127
Country: Italy
Email: antonio.loguercio@dedalus.eu
Phone: +393461188844

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JHTAP5VEZMYNPRA58AR73GZ5

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

Farmasafe@08055728030961
Farmasafe@08055728030855
FARMASAFE@08055728030671
FARMASAFE@08055728030336