Diagnostic Kit for Antibody and Antigen to Human Immunodeficiency Virus (Elisa) / 人类免疫缺陷病毒抗体抗原联合诊断试剂盒（酶联免疫法）
国药准字SJ20150002 · 诊断试剂盒
Statutory filing line: 2028-07-14
The certificate expires 2029-01-14. Under the Provisions for Drug Registration (药品注册管理办法) Art. 82, an application to renew is filed no later than 6 months before expiry.
| Approval number (批准文号) | 国药准字SJ20150002 |
|---|---|
| Generic name (通用名) | Diagnostic Kit for Antibody and Antigen to Human Immunodeficiency Virus (Elisa) 人类免疫缺陷病毒抗体抗原联合诊断试剂盒（酶联免疫法） |
| Marketing Authorisation Holder (上市许可持有人) | DiaSorin Italia S.p.A. UK Branch United Kingdom |
| Certificate valid until (有效期至) | 2029-01-14 |
| Filing line, Art. 82 (法定申报时限) | 2028-07-14 |
| Data as of (数据快照日) | 2026-06-28 |
All China registrations held by DiaSorin Italia S.p.A. UK Branch →
Check another product →Every figure above is taken from the public NMPA overseas-drug database (境外生产药品库) as of 2026-06-28, or computed from it under Art. 82. Registration data changes; the NMPA portal governs. This page states no view on whether this product’s Domestic Responsible Person (境内责任人) arrangement meets NMPA Announcement No. 137 — that cannot be determined from a single public entry.