PUREMED Pulse Oximeter - Indonesia BPOM Medical Device Registration
PUREMED Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502127661. The device is manufactured by SHENZHEN IMDK MEDICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ROYAL SEJAHTERA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN IMDK MEDICAL TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
ROYAL SEJAHTERA MANDIRIAR Address
Ruko Mahkota Ancol Blok E No.53, Jl. RE Martadinata, Kelurahan Pademanagn Barat
Registration Date
Sep 10, 2024
Expiry Date
Sep 10, 2027
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics

