CHIEFTAIN Syringe Pump - Indonesia BPOM Medical Device Registration
CHIEFTAIN Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902120708. The device is manufactured by BEIJING EASTERN CHIEFTAIN TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MOGA PRATAMA SUCCESS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING EASTERN CHIEFTAIN TECHNOLOGY CO.,LTD.Country of Origin
China
Authorized Representative
PT. MOGA PRATAMA SUCCESSAR Address
RUKO EMERALD COMERCIAL BLOK UB NO. 37 SUMARECON
Registration Date
Feb 02, 2021
Expiry Date
Sep 21, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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