LiliF Streptococcus pneumoniae Ag Rapid Kit - Indonesia BPOM Medical Device Registration
LiliF Streptococcus pneumoniae Ag Rapid Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321287. The device is manufactured by INTRON BIOTECHNOLOGY, INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NEXT LEVEL MEDICAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INTRON BIOTECHNOLOGY, INC.Country of Origin
Korea
Authorized Representative
PT. NEXT LEVEL MEDICALAR Address
JALAN BUKIT GADING RAYA, KOMPLEK GADING BUKIT INDAH, BLOK TB KAVLING NO. 30 LT.3
Registration Date
Jul 25, 2023
Expiry Date
Aug 02, 2025
Product Type
Serological Reagents
Streptococcus spp. serological reagents.
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