BOZTRON Patient Monitor - Indonesia BPOM Medical Device Registration
BOZTRON Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320856. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. KARINDO ALKESTRONAR Address
JL. TOMANG RAYA NO.17
Registration Date
Jun 30, 2023
Expiry Date
Jun 26, 2026
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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