SERENITY Fingertip Pulse Oximeter - Indonesia BPOM Medical Device Registration
SERENITY Fingertip Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502520022. The device is manufactured by JOYTECH HEALTCARE 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
JOYTECH HEALTCARE 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
Jan 06, 2025
Expiry Date
Feb 07, 2028
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics
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