GLOBUS® Magneto Therapy - Indonesia BPOM Medical Device Registration
GLOBUS® Magneto Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003716998. The device is manufactured by DOMINO S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SATYA ABADI VISIMED.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DOMINO S.R.L.Country of Origin
Italy
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 08, 2024
Expiry Date
Jul 20, 2028
Product Type
Therapeutic Neurology Equipment
Repetitive transcranial magnetic stimulation system
Non Radiation Electromedics
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