RAPIDAN TESTER Gonorrhea Test - Indonesia BPOM Medical Device Registration

RAPIDAN TESTER Gonorrhea Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303718816. The device is manufactured by TURKLAB TIBBI MALZEMELERI SAN, TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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BPOM Registered

Risk Class Kelas Resiko : C

RAPIDAN TESTER Gonorrhea Test

Analysis ID: AKL 20303718816

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

TURKLAB TIBBI MALZEMELERI SAN, TIC. A.S.

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 05, 2021

Expiry Date

Aug 27, 2026

Product Type

Serological Reagents

Neisseria spp. direct serological test reagents.

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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