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ALCORE Amphetamine (AMP) Rapid Test - Indonesia BPOM Medical Device Registration

ALCORE Amphetamine (AMP) Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103420325. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIMITRA DIAGNOSTICS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ALCORE Amphetamine (AMP) Rapid Test
Analysis ID: AKL 20103420325

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIMITRA DIAGNOSTICS INDONESIA

AR Address

JL. PANGERAN JAYAKARTA, RUKAN BUNTU WARGA NO.23A KEL.MANGGA DUA SELATAN KEC. SAWAH BESAR, JAKARTA PUSAT

Registration Date

Dec 04, 2024

Expiry Date

Dec 01, 2027

Product Type

Clinical Toxicology Test System

Amphetamine test system(card)

Invitro Diagnostics

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