ALLUX-Q - Indonesia BPOM Medical Device Registration
ALLUX-Q is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222274. The device is manufactured by AMI INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. STENIA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AMI INC.Country of Origin
Korea
Authorized Representative
PT. STENIA MEDIKAAR Address
GD. MASPION PLAZA LT.2 UNIT I JL. GUNUNG SAHARI RAYA KAV.18
Registration Date
Sep 22, 2022
Expiry Date
Jul 06, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
