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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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VIDAS® TBI (GFAP, UCH-L1) — 2 UDI-DI variants, IVDR (bioMérieux SA)

MD Atlas
bioMérieux SA

Data from EUDAMED, last updated May 19, 2026

VIDAS® TBI (GFAP, UCH-L1)

357302BUDI002001SS

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: bioMérieux SA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 357302BUDI002001SS
Device name: VIDAS® TBI (GFAP, UCH-L1)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: bioMérieux SA
SRN: FR-MF-000004436
Country: France
Email: media@biomerieux.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KR0TXPSFJ61PGQ2KZBX8P72J

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

VIDAS® TBI (GFAP, UCH-L1)03573026613860
VIDAS® TBI (GFAP, UCH-L1)03573026626884