ULTHERA SYSTEM PRIME - Indonesia BPOM Medical Device Registration
ULTHERA SYSTEM PRIME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421901. The device is manufactured by ULTHERA INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHARMINDO LESTARI AWARD.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ULTHERA INCCountry of Origin
United States
Authorized Representative
PT. PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M
Registration Date
Sep 17, 2024
Expiry Date
May 14, 2029
Product Type
Surgical Equipment
Focused ultrasound stimulator system for aesthetic use
Non Radiation Electromedics
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