ANCOOL Ultrasonic Pulmonary Function Testing - Indonesia BPOM Medical Device Registration
ANCOOL Ultrasonic Pulmonary Function Testing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401420018. The device is manufactured by ANCOOL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANCOOL TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
May 07, 2024
Expiry Date
Jan 02, 2027
Product Type
Diagnostic Anesthesia Equipment
Diagnostic spirometer.
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