DPMMED DPFusion VP1 Infusion Pump - Indonesia BPOM Medical Device Registration
DPMMED DPFusion VP1 Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902323033. The device is manufactured by CHANGSA 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
CHANGSA 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
Dec 20, 2023
Expiry Date
Jun 25, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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