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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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SARA — 2 UDI-DI variants, IVDR (DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.)

MD Atlas
DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.

Data from EUDAMED, last updated May 31, 2026

SARA

805061604INCS99

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 805061604INCS99
Device name: SARA
Device model: S.A.R.A.
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.
SRN: IT-MF-000029123
Country: Italy
Email: info@diapro.it
Phone: +390227007161

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KCGSFXDVTP428ZEJA76FS790

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

SARA_Gen208050616042767
SARA08050616042033