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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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Access TSH (3rd IS) — 2 UDI-DI variants, IVDR (IMMUNOTECH SAS )

MD Atlas
IMMUNOTECH SAS

Data from EUDAMED, last updated May 19, 2026

Access TSH (3rd IS)

150995903AccTSH3rdCL

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: IMMUNOTECH SAS

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 150995903AccTSH3rdCL
Device name: Access TSH (3rd IS)
Device model: B63284
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Mar 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: IMMUNOTECH SAS
SRN: FR-MF-000011121
Country: France
Email: sroquesviolin@beckman.com
Phone: 0620853085

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FYZJPYVW017F0NVY1DT9HJCV

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

Access TSH (3rd IS)15099590744373
Access TSH (3rd IS)15099590671495