CITODIA Multi Drug 7 Rapid Test Panel (AMP/THC/MOP/MET/BZO/COC/ K3 (AB-PINACA, AB-FUBINACA) - Indonesia BPOM Medical Device Registration
CITODIA Multi Drug 7 Rapid Test Panel (AMP/THC/MOP/MET/BZO/COC/ K3 (AB-PINACA, AB-FUBINACA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103917283. The device is manufactured by ACRO BIOTECH, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PROSPEROUS BIOCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACRO BIOTECH, INC.Country of Origin
United States
Authorized Representative
PT. PROSPEROUS BIOCAREAR Address
Taman Laguna Blok K3 No.3 RT.03 RW.02 Kel. Jatikarya, Kec. Jatisampurna Bekasi 17435
Registration Date
Nov 05, 2019
Expiry Date
Nov 30, 2023
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
Invitro Diagnostics
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