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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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Thrombo-Aggregometer — 2 UDI-DI variants, IVDR (SD Innovation)

MD Atlas
SD Innovation

Data from EUDAMED, last updated May 19, 2026

Thrombo-Aggregometer

3770025379TH-V3ZC

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: SD Innovation

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 3770025379TH-V3ZC
Device name: Thrombo-Aggregometer
Device model: TH-V3
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: SD Innovation
SRN: FR-MF-000003775
Country: France
Email: contact@sd-innovation.fr

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HMGHGZ16B8TR137ZN7KE8M9S

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

Thrombo-Aggregometer03770025379166
Thrombo-Aggregometer03770025379135