HEARTSTART FRx Defibrillator - Indonesia BPOM Medical Device Registration
HEARTSTART FRx Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505024852. The device is manufactured by PHILIPS MEDICAL SYSTEMS from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
PHILIPS MEDICAL SYSTEMSCountry of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Aug 30, 2020
Expiry Date
Jun 26, 2025
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
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