SEINOFY Covid-19 Antigen Rapid Test Cassette - Indonesia BPOM Medical Device Registration
SEINOFY Covid-19 Antigen Rapid Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303126970. The device is manufactured by ZHEJIANG ANJI SAIANFU BIOTECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOY INDO MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG ANJI SAIANFU BIOTECH CO.,LTDCountry of Origin
China
Authorized Representative
PT. JOY INDO MEDIKAAR Address
JALAN WR SUPRATMAN NOMOR 168
Registration Date
Nov 09, 2022
Expiry Date
Aug 25, 2026
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics
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