JUSCHEK Multi-Drug 3 Drug Rapid Test Panel - Indonesia BPOM Medical Device Registration
JUSCHEK Multi-Drug 3 Drug Rapid Test Panel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320311. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRACE REMAINS PROSPEROUS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. GRACE REMAINS PROSPEROUSAR Address
ANUGERAH TETAP MAKMUR
Registration Date
Mar 03, 2023
Expiry Date
Apr 21, 2027
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
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