IntraSight - Indonesia BPOM Medical Device Registration
IntraSight is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125157. The device is manufactured by KIMBALL ELECTRONICS LLC โ JASPER 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
KIMBALL ELECTRONICS LLC โ JASPERCountry of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Dec 12, 2022
Expiry Date
May 19, 2026
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed echo imaging system.
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