FORMASTER Multi-Drug Rapid Test (Urine Cup) MDMA500/AMP1000/BZO300/COC300/MTD300/KET1000/MET1000/MOP300/THC50/PCP25/APAP2000/K250(12 Parameter) - Indonesia BPOM Medical Device Registration
FORMASTER Multi-Drug Rapid Test (Urine Cup) MDMA500/AMP1000/BZO300/COC300/MTD300/KET1000/MET1000/MOP300/THC50/PCP25/APAP2000/K250(12 Parameter) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103420317. The device is manufactured by ANHUI FORMASTER BIOSCI CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NOVAMED BIOTECH INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANHUI FORMASTER BIOSCI CO., LTD.Country of Origin
China
Authorized Representative
PT. NOVAMED BIOTECH INDONESIAAR Address
Rukan Cluster Aerowalk blok C.01 No. 03 RT. 4/RW 8 , Aeroworld 8
Registration Date
Nov 22, 2024
Expiry Date
May 23, 2029
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
Invitro Diagnostics

