VIRTUE DX Syphilis TP Reagent Kit - Indonesia BPOM Medical Device Registration
VIRTUE DX Syphilis TP Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321274. The device is manufactured by VIRTUE DIAGNOSTICS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DARMA LABORA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIRTUE DIAGNOSTICS SUZHOU CO., LTD.Country of Origin
China
Authorized Representative
PT. DARMA LABORA INDONESIAAR Address
KAWASAN INDUSTRI JABABEKA 7, BLOK B3/B, DESA WANGUNHARJA
Registration Date
Jan 14, 2025
Expiry Date
Mar 02, 2028
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
Invitro Diagnostics
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VIRTUE DX Estradiol Reagent Kit
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