United Kingdom MHRA device registration 167562

Fibrinogen assay (factor I) IVD, kit, clotting

United Kingdom·In Vitro Diagnostic Device·Siemens Healthcare Diagnostics Products GmbH·Registered Nov 26, 2024

Registration details

Device ID: 167562
MHRA Reference Number: 167562
Date Registered: Nov 26, 2024
Last Updated: Aug 16, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Fibrinogen assay (factor I) IVD, kit, clotting
Type: Class C

Manufacturer

Name: Siemens Healthcare Diagnostics Products GmbH
Address: Emil-Von-Behring-Str. 76
Marburg, Germany
Created Date: Oct 8, 2021

Authorized Representative

Name: Siemens Healthcare Diagnostics Limited
Relationship Type: UK Responsible Person
Address: Park View Watchmoor Park
Surrey, Camberley, England, United Kingdom
Postcode: GU15 3YL

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About this record

Fibrinogen assay (factor I) IVD, kit, clotting is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 167562. The device is manufactured by Siemens Healthcare Diagnostics Products GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Siemens Healthcare Diagnostics Limited.

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