Pure Global

Shenzhen Kinghi Biotechnology Co., Ltd. - Medical Device Manufacturer in United Kingdom

Shenzhen Kinghi Biotechnology Co., Ltd. from China is a medical device manufacturer with 20 registered products in the UK MHRA database through Pure Global AI's free platform. The company produces 20 unique generic names across 1 device type.

This page provides comprehensive manufacturer intelligence including complete product portfolio and device type distribution. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify manufacturers, analyze portfolios, and discover partnership opportunities efficiently.

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20 Products
1 Types
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Shenzhen Kinghi Biotechnology Co., Ltd.
China

3B-1601, building 3, hengtaiyu building, Tangwei community, Fenghuang street, Guangming District

Shenzhen, China

20
Total Products
20
Generic Names
1
Device Types
20
Generic Names
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Recent Registrations (20 most recent)
Most recently registered products with MHRA

Cancer antigen 125 (CA125) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173375

Registration Date:

May 24, 2024

Cancer antigen 242 (CA242) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173409

Registration Date:

May 24, 2024

Cancer?antigen?19-9 (CA19-9) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173378

Registration Date:

May 24, 2024

Collagen type IV IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173411

Registration Date:

May 24, 2024

Creatine?kinase?myocardial?isoenzyme (CKMB) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173404

Registration Date:

May 24, 2024

D-dimer IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173385

Registration Date:

May 24, 2024

Estradiol?(oestradiol) (E2) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173362

Registration Date:

May 24, 2024

Hyaluronic acid (HA) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173413

Registration Date:

May 24, 2024

Interleukin-6 (IL-6) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173396

Registration Date:

May 24, 2024

Myoglobin IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173405

Registration Date:

May 24, 2024

Plasmin-alpha-2-antiplasmin complex (PAP) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173387

Registration Date:

May 24, 2024

Progastrin-releasing peptide (ProGRP) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173382

Registration Date:

May 24, 2024

Serum amyloid A IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173395

Registration Date:

May 24, 2024

Thrombin-antithrombin III complex (TAT) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173388

Registration Date:

May 24, 2024

Thrombomodulin IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173389

Registration Date:

May 24, 2024

Thyroglobulin antibody IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173357

Registration Date:

May 24, 2024

Thyroid peroxidase antibody (anti-TPO/microsomal antibody) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173358

Registration Date:

May 24, 2024

Tissue plasminogen activator-plasminogen activator inhibitor complex (tPA:PAI) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173390

Registration Date:

May 24, 2024

Total thyroxine (TT4) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173353

Registration Date:

May 24, 2024

Adrenocorticotropic hormone (ACTH) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

173403

Registration Date:

May 24, 2024