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RAPIDAN TESTER Malaria Test - Indonesia BPOM Medical Device Registration

RAPIDAN TESTER Malaria Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303714536. The device is manufactured by TURKLAB TIBBI MALZEMELERI SAN, TIC. A.S. from Turkey, 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
RAPIDAN TESTER Malaria Test
Analysis ID: AKL 20303714536

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

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

Dec 25, 2021

Expiry Date

Sep 07, 2026

Product Type

Serological Reagents

Plasmodium species antigen detection assays

Invitro Diagnostics

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