TIANLONG Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Fluorescence PCR Method) - Indonesia BPOM Medical Device Registration
TIANLONG Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Fluorescence PCR Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306220025. The device is manufactured by SUZHOU TIANLONG BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTERSKALA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU TIANLONG BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
INTERSKALA MEDIKA INDONESIAAR Address
Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18
Registration Date
Apr 23, 2022
Expiry Date
Jan 03, 2027
Product Type
Tumor Antigen Immunologic Test System
Dna Detection for Human Papillomavirus
Invitro Diagnostics
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