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RAPIDAN Tester HBsAg Test, WB/S/P - Indonesia BPOM Medical Device Registration

RAPIDAN Tester HBsAg Test, WB/S/P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305129811. The device is manufactured by TURKLAB TIBBI MALZEMELERI SAN, TIC. A.S from Turkey, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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BPOM Registered
Risk Class Kelas Resiko : D
RAPIDAN Tester HBsAg Test, WB/S/P
Analysis ID: AKL 30305129811

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

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 27, 2021

Expiry Date

Sep 07, 2026

Product Type

Immunological Test System

Antimitochondrial antibody immunological test system.

Invitro Diagnostics

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