SONOMED Vumax Ultrasound System - Indonesia BPOM Medical Device Registration
SONOMED Vumax Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125096. The device is manufactured by SONOMED INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SONOMED INCCountry of Origin
United States
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
Aug 19, 2021
Expiry Date
Oct 20, 2025
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed echo imaging system.
Non Radiation Electromedics
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