United Kingdom MHRA device registration 3721

2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, kit, enzyme immunoassay (EIA)

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

Registration details

Device ID: 3721
MHRA Reference Number: 3721
Date Registered: Nov 26, 2024
Last Updated: Aug 16, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: 2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: Siemens Healthcare Diagnostics Inc
Address: 511 Benedict Avenue
Tarrytown, NY, United States
Created Date: Oct 19, 2017

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

2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 3721. 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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