United Kingdom MHRA device registration 170483

Neisseria gonorrhoeae antigen IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Primer Design Ltd·Registered Oct 14, 2021

Registration details

Device ID: 170483
MHRA Reference Number: 170483
Date Registered: Oct 14, 2021
Last Updated: Apr 13, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Neisseria gonorrhoeae antigen IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Primer Design Ltd
Address: York House School Lane, Chandler's Ford, Eastleigh
Southampton, Hampshire, England, United Kingdom
Created Date: Jan 24, 2018

Similar products

Devices with a matching generic name or device type registered with MHRA

Alpha-fetoprotein (AFP) IVD, kit, fluorescent immunoassayN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176179

Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, fluorescent immunoassayN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176185

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinicalN/A

Type: In Vitro Diagnostic Device

Manufacturer: Primer Design Ltd

Device ID: 175386

Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassayN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176184

C-reactive protein (CRP) IVD, kit, fluorescent immunoassayN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176164

Cryptosporidium species antigen IVD, kit, rapid ICT, clinicalN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176139

Respiratory syncytial virus (RSV) antigen IVD, kit, rapid ICT, clinicalN/A

Type: In Vitro Diagnostic Device

Manufacturer: Primer Design Ltd

Device ID: 175389

SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testingN/A

Type: In Vitro Diagnostic Device

Manufacturer: Primer Design Ltd

Device ID: 175394

Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinicalN/A

Type: In Vitro Diagnostic Device

Manufacturer: Primer Design Ltd

Device ID: 175395

D-dimer IVD, kit, fluorescent immunoassayN/A

Type: In Vitro Diagnostic Device

Manufacturer: Vitrosens Biyoteknoloji A.S.

Device ID: 176162

Other products from Primer Design Ltd

Additional devices registered by the same manufacturer

Helicobacter pylori antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175388

Clostridium difficile antigen IVD, antibody

Type: In Vitro Diagnostic Device

Device ID: 175384

Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175393

SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

Type: In Vitro Diagnostic Device

Device ID: 175394

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175386

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175385

Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175395

Respiratory syncytial virus (RSV) antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175389

Dengue virus antigen/antibody IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175391

Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Device ID: 175387

About this record

Neisseria gonorrhoeae antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170483. The device is manufactured by Primer Design Ltd from England, United Kingdom, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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.

Free DatabasePowered by Pure Global AIMHRA RegisteredIn Vitro Diagnostic Device