HYBRIBIO DNA Hybrimax - Indonesia BPOM Medical Device Registration
HYBRIBIO DNA Hybrimax is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304220106. The device is manufactured by GUANGZHOU HYBRIBIO MEDICINE TECHNOLOGY LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BESTARI SUKSES MAKMUR.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU HYBRIBIO MEDICINE TECHNOLOGY LTDCountry of Origin
China
Authorized Representative
PT. BESTARI SUKSES MAKMURAR Address
KOKAN PERMATA KELAPA GADING LT. 3, BLOK E-5, JL. BOULEVARD GADING RAYA, KELAPA GADING BARAT, KELAPA GADING, JAKARTA UTARA
Registration Date
Aug 22, 2023
Expiry Date
Jan 01, 2026
Product Type
Immunology Laboratory Equipment and Reagents
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