MedioStar - Indonesia BPOM Medical Device Registration
MedioStar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325072. The device is manufactured by ASCLEPION LASER TECHNOLOGIES GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AESENDIA INFINI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASCLEPION LASER TECHNOLOGIES GMBHCountry of Origin
Germany
Authorized Representative
PT. AESENDIA INFINI INDONESIAAR Address
AESENDIA INFINI INDONESIA
Registration Date
Sep 21, 2023
Expiry Date
Jan 16, 2028
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
