WONDFO CK-MB Rapid Test - Indonesia BPOM Medical Device Registration
WONDFO CK-MB Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101815224. 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 EXXEL MAIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU WONDFO BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
EXXEL MAINAR Address
JALAN RAJAWALI SELATAN.RUKO MULTI GUNA KEMAYORAN BLOK.6N.JAKARTA UTARA
Registration Date
Apr 04, 2023
Expiry Date
Sep 08, 2026
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system (card)
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