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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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CACCIAVITE MANUALE — 19 UDI-DI variants, MDR (IDI EVOLUTION S.r.l.)

MD Atlas
IDI EVOLUTION S.r.l.

Data from EUDAMED, last updated May 30, 2026

CACCIAVITE MANUALE

805577346COMPACCESSORIARF

19 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: IDI EVOLUTION S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805577346COMPACCESSORIARF
Device name: CACCIAVITE MANUALE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: IDI EVOLUTION S.r.l.
SRN: IT-MF-000005920
Country: Italy
Email: qualita@idievolution.it

Variants by status

UDI-DI variants

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FSW4KDBEA4XD0YSFYGQA5B5D

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

60070908055773460171
60070808055773460164
60072908055773460188
90900708055773460072
90901008055773460096
90900908055773460089
90901208055773460102
51590208055773460065
51590008055773460058
90900708055773460119
90901008055773460133
90900908055773460126
90901208055773460140
90502308055773460027
90595508055773460041
90595008055773460034
90502108055773460010
60070308055773460157
90900408055773460003