SPIRIT Infusion Pump - Indonesia BPOM Medical Device Registration
SPIRIT Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127706. The device is manufactured by SINO MEDICAL-DEVICE TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MAIN SOURCE MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SINO MEDICAL-DEVICE TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
MAIN SOURCE MEDICALINDOAR Address
JL.PROF HM YAMIN SH NO.241 A SEI KERA HILIR I
Registration Date
Nov 12, 2024
Expiry Date
Nov 11, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics

