United Kingdom MHRA device registration 68711

Multiple drugs of abuse IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Guangzhou Wondfo Biotech Co., Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 68711
MHRA Reference Number: 68711
Date Registered: Nov 26, 2024
Last Updated: Jul 31, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Guangzhou Wondfo Biotech Co., Ltd.
Address: No.8 Lizhishan Road, Science City, Huangpu District
Guangzhou, China
Created Date: Mar 7, 2021

Authorized Representative

Name: Qarad UK Ltd.
Relationship Type: UK Responsible Person
Address: 8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY

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 Guangzhou Wondfo Biotech Co., Ltd.

Additional devices registered by the same manufacturer

Ultraviolet-visible spectrophotometer IVDMar 11, 2025

Type: In Vitro Diagnostic Device

Device ID: 212690

Rheumatoid factor IVD, kit, fluorescent immunoassayMar 11, 2025

Type: In Vitro Diagnostic Device

Device ID: 212687

Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, fluorescent immunoassayMar 11, 2025

Type: In Vitro Diagnostic Device

Device ID: 212688

Suppression of tumorigenicity 2 (ST2) IVD, kit, fluorescent immunoassayMar 11, 2025

Type: In Vitro Diagnostic Device

Device ID: 212686

Vitamin B12 IVD, kit, rapid ICT, clinicalMar 11, 2025

Type: In Vitro Diagnostic Device

Device ID: 212689

Activated partial thromboplastin time (APTT) IVD, reagentNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 170249

2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 170257

Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassayNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 170238

B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, controlNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 170194

Beta-2-microglobulin IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 170223

Other products from same authorized representative

Additional devices represented by Qarad UK Ltd. in the UK

SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Beijing Wantai Biological Pharmacy Enterprise Co., Ltd.

Device ID: 125922

SARS-CoV-2 immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Beijing Wantai Biological Pharmacy Enterprise Co., Ltd.

Device ID: 125920

Acute myeloid leukaemia (AML) genetic mutation IVD, kit, nucleic acid technique (NAT)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: BIOTYPE GmbH

Device ID: 192304

Influenza A/B virus antigen IVD, kit, rapid ICT, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: BIOSYNEX SWISS SA

Device ID: 165388

Multiple gastrointestinal virus antigen IVD, kit, rapid ICT, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: BIOSYNEX SWISS SA

Device ID: 165382

Total human chorionic gonadotropin (HCG) IVD, kit, immunochromatographic test (ICT), rapidNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: BIOSYNEX SWISS SA

Device ID: 165387

Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: BIOSYNEX SWISS SA

Device ID: 165386

Adeno-associated virus neutralizing antibody IVD, kit, bioassayNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Precision for Medicine

Device ID: 93376

General specimen collection kit IVD, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Precision for Medicine

Device ID: 163628

Interferon gamma release IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Beijing Wantai Biological Pharmacy Enterprise Co., Ltd.

Device ID: 125918

About this record

Multiple drugs of abuse IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68711. The device is manufactured by Guangzhou Wondfo Biotech Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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.

Free DatabasePowered by Pure Global AIMHRA RegisteredIn Vitro Diagnostic Device