DP Fusion SP1 Syringe Pump - Indonesia BPOM Medical Device Registration
DP Fusion SP1 Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127407. 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 INDOPRIMA BIONET.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHANGSA DEEPMED MEDICAL TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
Nov 29, 2021
Expiry Date
Jan 27, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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