PHILIPS Ultrasound System 3300 - Indonesia BPOM Medical Device Registration
PHILIPS Ultrasound System 3300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501026138. The device is manufactured by NEUSOFT MEDICAL SYSTEM CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEUSOFT MEDICAL SYSTEM CO., LTDCountry of Origin
China
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Oct 13, 2020
Expiry Date
Jun 22, 2025
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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