United Kingdom MHRA device registration 168229

Instrument/analyser specimen/reagent container carrier IVD

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Siemens Healthcare Diagnostics Inc·Registered Nov 26, 2024
Registration details
Device ID
168229
MHRA Reference Number
168229
Date Registered
Nov 26, 2024
Last Updated
Aug 16, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Instrument/analyser specimen/reagent container carrier IVD
Type
Class A
Manufacturer
Address
511 Benedict Avenue
Tarrytown, NY, United States
Created Date
Oct 19, 2017
Authorized Representative
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

Instrument/analyser specimen/reagent container carrier IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168229. The device is manufactured by Siemens Healthcare Diagnostics Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Siemens Healthcare Diagnostics Limited.

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