Novel Coronavirus 2019-nCoV Rapid Detection Kit (LAMP)

中|EN

Products and Services

Introduction

Certifications: CE certification, Philippines, and Thailand FDA certification, Import License of UAE
Usage

This kit is used for in vitro qualitative and rapid detection of (2019-nCoV) ORF1ab gene in human nasopharyngeal swab samples.
Product Information

Packaging Size: 96 tests/kit
Sample Requirements

Storage Conditions: The collected samples shall be submitted for detection in time.

Validity Period: 2-8ºC, 24 hours;
Below -70ºC: 6 months, avoid repeated freezing and thawing.
Requirements of Sample Processing:
1. Nasopharyngeal swab: nucleic acid extraction or inactivation treatment.
2. Throat swab: nucleic acid extraction.
Storage Conditions and Validity Period

Storage Conditions: -20±5°C
Validity Period: stated on the label of each product.

Links

State-owned Assets Supervision and Administration Commission of the State Council National Health Commission of the People's Republic of China National Healthcare Security Administration State Administration for Market Regulation National Medical Products Administration (NMPA) Sinopharm Group China National Biotech Group Changchun Institute of Biological Products Co., Ltd PathoFinder GeneoDx Yaxin Bio

Tel: 400-9880-666

Address: 1 / F, Building 3, 218 Yindu Road, Xuhui District, Shanghai

Business Opportunity: inquiry_GeneoDx@sinopharm.com

International Cooperation: imd@geneodx.com

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