NISSEI Pulse Oximeter - Indonesia BPOM Medical Device Registration
NISSEI Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502917307. The device is manufactured by NIHON SEIMITSU SOKKI CO.,LTD from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIHON SEIMITSU SOKKI CO.,LTDCountry of Origin
Japan
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Apr 16, 2024
Expiry Date
Mar 01, 2029
Product Type
Monitoring Cardiology Equipment
Oximeter.
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