Hokap™ FT4 - Indonesia BPOM Medical Device Registration
Hokap™ FT4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220051. The device is manufactured by SUZHOU HOKAPI BIOMEDICAL ENGINEERING CO., LTD, CHINA. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Dec 03, 2023
Expiry Date
Dec 31, 2025
Product Type
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