Pure Global

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

Shenzhen Channel 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 Channel Biotechnology Co., Ltd.
China

701, East Block, 9th Building, Tianliao Industrial Zone A, Taoyuan Street, Nanshan District

Shenzhen, Guangdong, China

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

Multiple form 25-hydroxy vitamin D IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167513

Registration Date:

Nov 26, 2024

Thyroid stimulating hormone (TSH) IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

167506

Registration Date:

Nov 26, 2024

Troponin I IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167509

Registration Date:

Nov 26, 2024

Vitamin B12 IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167514

Registration Date:

Nov 26, 2024

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

Type:

In Vitro Diagnostic Device

Device ID:

167511

Registration Date:

Nov 26, 2024

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

Type:

In Vitro Diagnostic Device

Device ID:

167499

Registration Date:

Nov 26, 2024

Follicle stimulating hormone (FSH) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167496

Registration Date:

Nov 26, 2024

Free triiodothyronine (FT3) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

163249

Registration Date:

Nov 26, 2024

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167494

Registration Date:

Nov 26, 2024

Myoglobin IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167510

Registration Date:

Nov 26, 2024

Progesterone IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167492

Registration Date:

Nov 26, 2024

Prolactin IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167497

Registration Date:

Nov 26, 2024

Thyroglobulin antibody IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167504

Registration Date:

Nov 26, 2024

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

Type:

In Vitro Diagnostic Device

Device ID:

167505

Registration Date:

Nov 26, 2024

Thyroid stimulating hormone (TSH) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167493

Registration Date:

Nov 26, 2024

Total estriol (oestriol) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167498

Registration Date:

Nov 26, 2024

Total testosterone IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167500

Registration Date:

Nov 26, 2024

Total thyroxine (TT4) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167502

Registration Date:

Nov 26, 2024

B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167512

Registration Date:

Nov 26, 2024

Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

167491

Registration Date:

Nov 26, 2024