SERENITY Infusion Pump - Indonesia BPOM Medical Device Registration
SERENITY Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902810057. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENTS 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 COMEN MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Sep 04, 2022
Expiry Date
Apr 06, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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VIECARE Defibrillator Monitor
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COMEN Fan
SERENITY Patient Monitor
MEDINA Fetal Maternal Monitor
MEDINA Advance Modular Monitor
MEDINA Incubator
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