SERENITY Defibrillator - Indonesia BPOM Medical Device Registration
SERENITY Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505320283. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD.Country 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
Sep 29, 2023
Expiry Date
Feb 08, 2028
Product Type
Therapeutic Cardiology Equipment
DC-defibrillator (including paddles).
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