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ANSWER AMP One Step Amphetamine Test Device - Indonesia BPOM Medical Device Registration

ANSWER AMP One Step Amphetamine Test Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103121059. The device is manufactured by ABON BIOPHARM (HANGZOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EXXEL MAIN.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
ANSWER AMP One Step Amphetamine Test Device
Analysis ID: AKL 20103121059

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. EXXEL MAIN

AR Address

JALAN RAJAWALI SELATAN.RUKO MULTI GUNA KEMAYORAN BLOK.6N.JAKARTA UTARA

Registration Date

May 28, 2023

Expiry Date

May 26, 2026

Product Type

Clinical Toxicology Test System

Amphetamine test system(card)

Invitro Diagnostics

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