MASIMO iSpO2® Pulse Oximeter - Indonesia BPOM Medical Device Registration
MASIMO iSpO2® Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502814563. 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 MADESA SEJAHTERA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MASIMO CORPORATION.Country of Origin
United States
Authorized Representative
MADESA SEJAHTERA UTAMAAR Address
JL. GUNUNG SAHARI RAYA 51- A NO.14
Registration Date
Nov 14, 2022
Expiry Date
Dec 31, 2025
Product Type
Monitoring Cardiology Equipment
Oximeter.
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