MISONIX Sonastar Ultrasonic Surgical Asporation System - Indonesia BPOM Medical Device Registration
MISONIX Sonastar Ultrasonic Surgical Asporation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420411. The device is manufactured by MISONIX INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MISONIX INC.Country of Origin
United States
Authorized Representative
PT. SIGMA KARSA MAGNAAR Address
Ruko Mega Grosir Cempaka Mas, Jl. Letjen Suprapto Blok J No. 37-38 RW.08, Kel. Sumur Batu, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Feb 19, 2024
Expiry Date
Sep 12, 2027
Product Type
Surgical Equipment
Ultrasonic surgical instrument
Non Radiation Electromedics
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