TIANLONG Mycoplasma Pneumoniae (MP) Nucleic Acid Detection Kit (Fluorescence PCR Method) - Indonesia BPOM Medical Device Registration
TIANLONG Mycoplasma Pneumoniae (MP) 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 20303420487. The device is manufactured by SUZHOU TIANLONG BIOTECHNOLOGY, CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTERSKALA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU TIANLONG BIOTECHNOLOGY, CO., LTDCountry of Origin
China
Authorized Representative
PT. INTERSKALA MEDIKA INDONESIAAR Address
Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18
Registration Date
Oct 07, 2024
Expiry Date
Dec 31, 2026
Product Type
Serological Reagents
Mycoplasma spp. serological reagents.
Invitro Diagnostics
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