ABON MDMA One Step Ecstasy Test Device (Urine) - Indonesia BPOM Medical Device Registration
ABON MDMA One Step Ecstasy Test Device (Urine) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103611933. The device is manufactured by ABON BIOPHARM (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ALERE HEALTH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ABON BIOPHARM (HANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
ALERE HEALTHAR Address
K-Link Tower Lantai 18 Zona D, E, dan F Jl. Gatot Subroto Kav. 59 A RT 001 RW 003 Kel. Kuningan Timur, Kec. Setiabudi, Jakarta Selatan
Registration Date
Nov 17, 2022
Expiry Date
Jul 04, 2027
Product Type
Clinical Toxicology Test System
Methamphetamine test system (strip & midstream)
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