SERENITY Pulse Oximeter - Indonesia BPOM Medical Device Registration
SERENITY Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502914772. The device is manufactured by SHENZHEN JUMPER MEDICAL EQUIPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN JUMPER MEDICAL EQUIPMENT CO., LTDCountry of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
Jul 24, 2023
Expiry Date
Feb 07, 2028
Product Type
Monitoring Cardiology Equipment
Oximeter.
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