MEDIATECH Pompa Asi Manual - Indonesia BPOM Medical Device Registration
MEDIATECH Pompa Asi Manual is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11104124467. The device is manufactured by NINGBO REAL BUBEE MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDIA TECHNOLOGY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
NINGBO REAL BUBEE MEDICAL EQUIPMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. MEDIA TECHNOLOGYAR Address
KOMPLEK INKOPAL BLOK C NO.71 JL.BOULEVARD BARAT RAYA, KEL.KELAPA GADING
Registration Date
Jun 24, 2024
Expiry Date
Jun 24, 2027
Product Type
Therapeutic Obstetric and Gynecological Equipment
Nonpowered breast pump.
Non Electromedic Non Sterile
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