PLANMED SOPHIE CLASSIC S - Indonesia BPOM Medical Device Registration
PLANMED SOPHIE CLASSIC S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501817794. The device is manufactured by PLANMED LTD. from Finland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SATYA ABADI VISIMED.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PLANMED LTD.Country of Origin
Finland
Authorized Representative
SATYA ABADI VISIMEDAR Address
Ruko Sentra Menteng Blok MN-28 Bintaro Jaya Sektor 7 Pondok Jaya Pondok Aren Tangerang 15224
Registration Date
Jan 02, 2025
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Radiology Equipment
Mammographic x-ray system.
Electromedic Radiation
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