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BOSON BIOTECH Rapid Benzodiazepine Test Card - Indonesia BPOM Medical Device Registration

BOSON BIOTECH Rapid Benzodiazepine Test Card is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103713191. The device is manufactured by XIAMEN BOSON BIOTECH CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is NELTA MULTI GRACIA.

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
BOSON BIOTECH Rapid Benzodiazepine Test Card
Analysis ID: AKL 20103713191

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

NELTA MULTI GRACIA

AR Address

Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960

Registration Date

Jun 20, 2023

Expiry Date

Nov 21, 2025

Product Type

Clinical Toxicology Test System

Benzodiazepine test system(card)

Invitro Diagnostics

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