SPIRIT Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration
SPIRIT Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220029. The device is manufactured by NINGBO YINZHOU XIANFENG ELECTRONICS INSTRUMENT FACTORY from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN SOURCE MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
PT. MAIN SOURCE MEDICALINDOAR Address
JL.PROF HM YAMIN SH NO.241 SEI KERA HILIR I
Registration Date
May 31, 2022
Expiry Date
May 30, 2025
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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