Pure Global

ALLCHEK™ Multi-Drug 3 Drugs Rapid Test Panel (AMP300/MOP300/THC50-(Urine) - Indonesia BPOM Medical Device Registration

ALLCHEK™ Multi-Drug 3 Drugs Rapid Test Panel (AMP300/MOP300/THC50-(Urine) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103220184. The device is manufactured by HANGZHOU ALLTEST BIOTECH, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SAMUDERA INTI MEDISINDO.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
ALLCHEK™ Multi-Drug 3 Drugs Rapid Test Panel (AMP300/MOP300/THC50-(Urine)
Analysis ID: AKL 20103220184

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SAMUDERA INTI MEDISINDO

AR Address

SAMUDERA INTI MEDISINDO

Registration Date

Nov 22, 2022

Expiry Date

Jul 30, 2027

Product Type

Clinical Toxicology Test System

Multi parameter clinical toxicology test system

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing