FEAS ELECTRONICA Defibrillator Monitor 3850B - Indonesia BPOM Medical Device Registration
FEAS ELECTRONICA Defibrillator Monitor 3850B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505711623. The device is manufactured by FEAS ELECTRONICA SA. from Argentina, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BINTANG SARANA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FEAS ELECTRONICA SA.Country of Origin
Argentina
Authorized Representative
PT. BINTANG SARANA MEDIKAAR Address
KOMPLEK RUKAN MEDIKAL E/2 RT 001 RW 001 KELURAHAN PONDOK KELAPA KECAMATAN DUREN SAWIT 13450
Registration Date
Sep 21, 2022
Expiry Date
Mar 23, 2027
Product Type
Therapeutic Cardiology Equipment
DC-defibrillator (including paddles).
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