PHILIPS Diagnostic Ultrasound System - Indonesia BPOM Medical Device Registration
PHILIPS Diagnostic Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501318196. The device is manufactured by PHILIPS HEALTHCARE (SUZHOU) CO. LTD. from China, 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 HEALTHCARE (SUZHOU) CO. LTD.Country of Origin
China
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005
Registration Date
Sep 10, 2024
Expiry Date
Mar 16, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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