Patient Information Center iX - Indonesia BPOM Medical Device Registration
Patient Information Center iX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501025454. The device is manufactured by PHILIPS MEDICAL SYSTEMS from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHILIPS MEDICAL SYSTEMSCountry of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005
Registration Date
Oct 16, 2024
Expiry Date
Jul 10, 2028
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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