WITLEAF Handheld Pulse Oximeter S300 - Indonesia BPOM Medical Device Registration
WITLEAF Handheld Pulse Oximeter S300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502129220. The device is manufactured by SHENZHEN WITLEAF MEDICAL ELECTRONICS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDONESIAN MEDICAL INNOVATION.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN WITLEAF MEDICAL ELECTRONICS CO., LTDCountry of Origin
China
Authorized Representative
PT. INDONESIAN MEDICAL INNOVATIONAR Address
Taman Buaran Indah I, Blok W/400
Registration Date
Dec 31, 2021
Expiry Date
Dec 31, 2023
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics
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