BERIGHT™ COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) - Indonesia BPOM Medical Device Registration
BERIGHT™ COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303120944. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MAIN ONCOPROBE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTDCountry of Origin
China
Authorized Representative
MAIN ONCOPROBEAR Address
APRT.ISTANA HARMONI LT.DASAR UNIT 1M, KOMP.HARMONI PLAZA JL.SURYOPRANOTO NO.2, PETOJO UTARA
Registration Date
Feb 28, 2022
Expiry Date
Nov 05, 2025
Product Type
Serological Reagents
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