PLUSLIFE HPV 16/18/45 Card - Indonesia BPOM Medical Device Registration
PLUSLIFE HPV 16/18/45 Card is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320246. The device is manufactured by GUANGZHOU PLUSLIFE BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU PLUSLIFE BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
Jl. Tanah Abang II No. 37 RT.001/RW.003, Kode Pos 10160, Kel. Petojo Selatan, Kec. Gambir, Kota Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Jul 18, 2023
Expiry Date
Jan 11, 2028
Product Type
Tumor Antigen Immunologic Test System
Dna Detection for Human Papillomavirus
Invitro Diagnostics
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