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VivaDiag™ C-Reactive Protein Control Solution - Indonesia BPOM Medical Device Registration

VivaDiag™ C-Reactive Protein Control Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305125509. The device is manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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
VivaDiag™ C-Reactive Protein Control Solution
Analysis ID: AKL 20305125509

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN MEDICAL CHAKRA

AR Address

KOMPLEK GOLDEN BOULEVARD BLOK G2 / 30 BSD CITY KEL. LENGKONG KARYA KEC. SERPONG UTARA TANGERANG SELATAN

Registration Date

Sep 08, 2021

Expiry Date

Sep 10, 2025

Product Type

Immunological Test System

C-reactive protein immunological test system.

Invitro Diagnostics

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DJ Fang

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