FORMASTER Multi-Drug Rapid test (Urine) MDMA 500/BZO 300/COC 300/APAP 2000/THC 50/K2 50/MOP 300/KET 1000 - Indonesia BPOM Medical Device Registration
FORMASTER Multi-Drug Rapid test (Urine) MDMA 500/BZO 300/COC 300/APAP 2000/THC 50/K2 50/MOP 300/KET 1000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103420316. 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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
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 20, 2024
Expiry Date
May 23, 2029
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
Invitro Diagnostics

