Platelet aggregation study IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

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.

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Platelet aggregation study IVD, kit, nephelometry/turbidimetry

MHRA Device ID: 151822•Ref: 151822

Device Type

In Vitro Diagnostic Device

Devices

Platelet aggregation study IVD, kit, nephelometry/turbidimetry

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 5, 2023

Manufacturer Information

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

DJ Fang

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Platelet aggregation study IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

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