ATIERE Intensive - Indonesia BPOM Medical Device Registration
ATIERE Intensive is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420058. The device is manufactured by MEDYTOX INC from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDYTOX INCCountry of Origin
Korea
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Jun 12, 2024
Expiry Date
Jan 23, 2029
Product Type
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