ALPHAMED Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration
ALPHAMED Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502123235. The device is manufactured by UTECH.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
UTECH.,LTDCountry of Origin
China
Authorized Representative
PT. CIPTA MEDIKA INDONESIAAR Address
GRAND UNEDO JL. BINA MARGA NO. 94 G
Registration Date
Jun 03, 2021
Expiry Date
Jun 02, 2024
Product Type
Monitoring Cardiology Equipment
Oximeter.
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