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 20902421102. 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
Jl. Taman Sari Raya, No. 56B, Tamansari
Registration Date
Sep 30, 2024
Expiry Date
Jun 24, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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