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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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Chorus BETA 2-GLYCOPROTEIN-M — 2 UDI-DI variants, IVDR

MD Atlas
DIESSE Diagnostica Senese S.p.A

Data from EUDAMED, last updated May 31, 2026

Chorus BETA 2-GLYCOPROTEIN-M

803389132CHORUSBGM005B

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: DIESSE Diagnostica Senese S.p.A

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Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 803389132CHORUSBGM005B
Device name: Chorus BETA 2-GLYCOPROTEIN-M
Device model: CHORUSBGM
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: DIESSE Diagnostica Senese S.p.A
SRN: IT-MF-000013311
Country: Italy
Email: qualita@diesse.it

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KFNE9461JWW777Q68DZVCQ19

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

86052/1208033891329303
8605208033891323370