Pure Global

Sansure Biotech Inc. - Medical Device Manufacturer in United Kingdom

Sansure Biotech Inc. 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
๐Ÿ‡ฌ๐Ÿ‡ง
Sansure Biotech Inc.
China

No. 680, Lusong Road, Yuelu District

Changsha , 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

Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

156598

Registration Date:

Nov 26, 2024

Chemiluminescent immunoassay analyser IVD

Type:

In Vitro Diagnostic Device

Device ID:

183188

Registration Date:

Nov 26, 2024

Hepatitis C virus nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

154421

Registration Date:

Nov 26, 2024

Herpes simplex virus 1 & 2 (HSV1 & 2) nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

154424

Registration Date:

Nov 26, 2024

Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

180607

Registration Date:

Nov 26, 2024

Human papillomavirus (HPV) nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

97701

Registration Date:

Nov 26, 2024

Multiple respiratory disease-associated bacteria nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

97697

Registration Date:

Nov 26, 2024

Mycoplasma genitalium nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

154428

Registration Date:

Nov 26, 2024

Mycoplasma pneumoniae nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

125624

Registration Date:

Nov 26, 2024

Myoglobin IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

183184

Registration Date:

Nov 26, 2024

Neisseria gonorrhoeae nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

180613

Registration Date:

Nov 26, 2024

Nucleic acid extraction/isolation kit IVD

Type:

In Vitro Diagnostic Device

Device ID:

97695

Registration Date:

Nov 26, 2024

Nucleic acid sample preparation instrument IVD

Type:

In Vitro Diagnostic Device

Device ID:

125629

Registration Date:

Nov 26, 2024

Procalcitonin (PCT) IVD, kit, chemiluminescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

183187

Registration Date:

Nov 26, 2024

SARS-CoV-2 neutralizing antibody IVD, kit, rapid ICT, clinical

Type:

In Vitro Diagnostic Device

Device ID:

132050

Registration Date:

Nov 26, 2024

SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid

Type:

In Vitro Diagnostic Device

Device ID:

97693

Registration Date:

Nov 26, 2024

SARS-CoV-2/influenza A/B nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

97694

Registration Date:

Nov 26, 2024

Streptococcus pneumoniae nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

156600

Registration Date:

Nov 26, 2024

Thermal cycler nucleic acid amplification analyser IVD, point-of-care

Type:

In Vitro Diagnostic Device

Device ID:

97692

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:

183183

Registration Date:

Nov 26, 2024