WONDFO hsCRP Rapid Test - Indonesia BPOM Medical Device Registration
WONDFO hsCRP Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305815444. The device is manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EXXEL MAIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU WONDFO BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. EXXEL MAINAR Address
JALAN RAJAWALI SELATAN.RUKO MULTI GUNA KEMAYORAN BLOK.6N.JAKARTA UTARA
Registration Date
Apr 19, 2023
Expiry Date
Sep 08, 2026
Product Type
Immunological Test System
C-reactive protein immunological test system.
Invitro Diagnostics
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