DP Fusion SP1S Syringe Pump - Indonesia BPOM Medical Device Registration
DP Fusion SP1S Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902022151. The device is manufactured by CHANGSHA DEEPMED MEDICAL 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
CHANGSHA DEEPMED MEDICAL 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
Jul 02, 2020
Expiry Date
Jan 01, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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