PHILIPS Ultrasound System 5300G - Indonesia BPOM Medical Device Registration
PHILIPS Ultrasound System 5300G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321082. The device is manufactured by PHILIPS ULTRASOUND LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHILIPS ULTRASOUND LLCCountry of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Apr 16, 2024
Expiry Date
Mar 16, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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