MASIMO Patient SafetyNet™* - Indonesia BPOM Medical Device Registration
MASIMO Patient SafetyNet™* is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502123091. The device is manufactured by MASIMO CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MADESA SEJAHTERA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MASIMO CORPORATION.Country of Origin
United States
Authorized Representative
PT. MADESA SEJAHTERA UTAMAAR Address
JL. GUNUNG SAHARI RAYA 51- A NO.14
Registration Date
Dec 08, 2023
Expiry Date
Dec 31, 2025
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics
MASIMO Rad-97 Pulse CO-Oximeter with Noninvasive Blood Pressure (NiBP)
MASIMO Rainbow SET® IntelliVue Module
MASIMO Radical 7 Pulse CO-Oximeter
MASIMO Rad-G™ Continuous Pulse Oximeter
MASIMO Rad-97 Pulse CO-Oximeter
MASIMO Radius PPG™ Tetherless Pulse Oximetry
NOMOLINE® ISA CO2
MASIMO Root™ Monitor
MASIMO Rad-G Pulse Oximeter
MASIMO Rad-57® Pulse CO-Oximeter
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