SANSURE Chlamydia Trachomatis/ Ureaplasma Urealyticum/ Neisseria Gonorrhoeae DNA Diagnostic Kit (PCR-Fluorescence Probing) - Indonesia BPOM Medical Device Registration
SANSURE Chlamydia Trachomatis/ Ureaplasma Urealyticum/ Neisseria Gonorrhoeae DNA Diagnostic Kit (PCR-Fluorescence Probing) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321021. The device is manufactured by SANSURE BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SANSURE BIOTECH INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SANSURE BIOTECH INCCountry of Origin
China
Authorized Representative
PT. SANSURE BIOTECH INDONESIAAR Address
SANSURE BIOTECH INDONESIA
Registration Date
Mar 10, 2023
Expiry Date
Dec 30, 2026
Product Type
Serological Reagents
Chlamydia serological reagents.
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