United Kingdom MHRA device registration 151822

Platelet aggregation study IVD, kit, nephelometry/turbidimetry

United Kingdom·In Vitro Diagnostic Device·Takeda Austria GmbH·Registered Nov 26, 2024

Registration details

Device ID: 151822
MHRA Reference Number: 151822
Date Registered: Nov 26, 2024
Last Updated: Oct 5, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Platelet aggregation study IVD, kit, nephelometry/turbidimetry
Type: IVD General

Manufacturer

Name: Takeda Austria GmbH
Address: St. Peter-Strasse 25
Linz, Upper Austria, Austria
Created Date: Jul 12, 2022

Authorized Representative

Name: MT Promedt Consulting Ltd
Relationship Type: UK Responsible Person
Address: Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP

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About this record

Platelet aggregation study IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 151822. The device is manufactured by Takeda Austria GmbH from Austria, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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