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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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FRESA DA CENTRO — 6 UDI-DI variants, MDR (IDI EVOLUTION S.r.l.)

MD Atlas
IDI EVOLUTION S.r.l.

Data from EUDAMED, last updated May 31, 2026

FRESA DA CENTRO

805577346FRESEHR

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: IDI EVOLUTION S.r.l.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 805577346FRESEHR
Device name: FRESA DA CENTRO
Device model: FDC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 5, 2025

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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K4D1WG55TMAJCH08KS5G9Q2D

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

506602N08055773463707
50660208055773461611
51020008055773464452
500603N08055773463271
50060108055773460959
50060208055773460966