Streptococcus pneumoniae antigen IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Streptococcus pneumoniae antigen IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138162. The device is manufactured by Quidel Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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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Streptococcus pneumoniae antigen IVD, kit, fluorescent immunoassay

MHRA Device ID: 138162•Ref: 138162

Device Type

In Vitro Diagnostic Device

Devices

Streptococcus pneumoniae antigen IVD, kit, fluorescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2023

Manufacturer Information

Name

Quidel Corporation

Address

10165 McKellar Ct.

San Diego CA, United States

Created Date

Feb 25, 2022

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Streptococcus pneumoniae antigen IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

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