B125 Patient Monitor - Indonesia BPOM Medical Device Registration
B125 Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501911047. The device is manufactured by CRITIKON DE MEXICO S. DE R.L. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CRITIKON DE MEXICO S. DE R.L. DE C.V.Country of Origin
Mexico
Authorized Representative
GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430
Registration Date
Apr 19, 2023
Expiry Date
Mar 13, 2028
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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