AUTOCHECK Ultrasound System - Indonesia BPOM Medical Device Registration
AUTOCHECK Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420830. The device is manufactured by ACO HEALTHCARE CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL ENERGY ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACO HEALTHCARE CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
PT. GLOBAL ENERGY ALKESINDOAR Address
Cengkareng Business City (CBC) Tower F Lt. 6, Jl. Atang Sanjaya No. 21, Kel. Benda, Kec. Benda, Kota Tangerang, Provinsi Banten 15125
Registration Date
Nov 22, 2024
Expiry Date
Nov 21, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD
AUTOCHECK Ultrasound System
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AUTOCHECK Ultrasound System
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AUTOCHECK Ultrasound System
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AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD
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