SENTEC Digital Monitor - Indonesia BPOM Medical Device Registration
SENTEC Digital Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402027726. The device is manufactured by SENTEC AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SENTEC AGCountry of Origin
Switzerland
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
jl.Ciputat Raya no 14 B.Pondok Pinang
Registration Date
Dec 15, 2022
Expiry Date
Oct 17, 2027
Product Type
Monitoring Anesthesia Equipment
Cutaneous carbon dioxide (PcCO2) monitor.
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