United Kingdom MHRA device registration 137236

Adrenocorticotropic hormone (ACTH) IVD, calibrator

United Kingdom·In Vitro Diagnostic Device·NeoMedica doo·Registered Apr 11, 2024

Registration details

Device ID: 137236
MHRA Reference Number: 137236
Date Registered: Apr 11, 2024
Last Updated: Oct 17, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Adrenocorticotropic hormone (ACTH) IVD, calibrator
Type: IVD General

Manufacturer

Name: NeoMedica doo
Address: Bulevar Svetog Cara Konstantina 82-86,
Nis, Serbia
Created Date: Nov 26, 2020

Authorized Representative

Name: Wellkang Ltd
Relationship Type: Authorised Representative (Northern Ireland)
Address: Enterprise Hub, NW Business Complex 1 Beraghmore Road
Derry, Northern Ireland, Northern Ireland, United Kingdom
Postcode: BT48 8SE

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 NeoMedica doo

Additional devices registered by the same manufacturer

Aldosterone IVD, calibratorApr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137229

Aldosterone IVD, controlApr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137230

Aldosterone IVD, kit, enzyme immunoassay (EIA)Apr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137180

Allergen-specific immunoglobulin E (IgE) antibody IVD, controlApr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137198

Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA)Apr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137085

Alpha-fetoprotein (AFP) IVD, controlApr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137222

Anti-Mullerian hormone (AMH) IVD, controlApr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137227

Aspergillus fumigatus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)Apr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137282

Borrelia afzelii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)Apr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137287

17-Hydroxyprogesterone IVD, kit, enzyme immunoassay (EIA)Apr 11, 2024

Type: In Vitro Diagnostic Device

Device ID: 137064

Other products from same authorized representative

Additional devices represented by Wellkang Ltd in the UK

Glucose monitoring system IVD, home-useNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: AEON DIAGNOSTIC Technology Corporation

Device ID: 156246

Faecal occult blood IVD, kit, rapid ICT, self-testingNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Abiores Technology (Beijing) Co., Ltd.

Device ID: 144277

SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, rapid ICT, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Abiores Technology (Beijing) Co., Ltd.

Device ID: 147932

SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinicalNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: Abiores Technology (Beijing) Co., Ltd.

Device ID: 147934

Clostridium difficile nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: 3B BlackBio Biotech India Limited (a subsidiary of Kilpest India Limited)

Device ID: 148429

Leukaemia-associated fusion gene IVD, controlNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: 3B BlackBio Biotech India Limited (a subsidiary of Kilpest India Limited)

Device ID: 147336

Leukaemia-associated fusion gene IVD, kit, nucleic acid technique (NAT)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: 3B BlackBio Biotech India Limited (a subsidiary of Kilpest India Limited)

Device ID: 148426

Microbiological transport medium IVDNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: 3B BlackBio Biotech India Limited (a subsidiary of Kilpest India Limited)

Device ID: 148435

Multiple-type gastrointestinal pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: 3B BlackBio Biotech India Limited (a subsidiary of Kilpest India Limited)

Device ID: 148428

Glucose analyser IVD, home-useNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: AEON DIAGNOSTIC Technology Corporation

Device ID: 156247

About this record

Adrenocorticotropic hormone (ACTH) IVD, calibrator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 137236. The device is manufactured by NeoMedica doo from Serbia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang 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