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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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SIM.CE — 1 UDI-DI variant, IVDD (DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.)

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

Data from EUDAMED, last updated May 31, 2026

SIM.CE

B-08050616040909

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — General

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Manufacturer: DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.

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Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: B-08050616040909
Device name: —
Device model: SIM.CE
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Version date: May 21, 2026

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

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS50G81YFCBWRK3K6RJED4RM

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

SYPH IgM08050616040909