MISONIX BONESCALPEL Ultrasonic OsteoSurgery System - Indonesia BPOM Medical Device Registration
MISONIX BONESCALPEL Ultrasonic OsteoSurgery System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303611447. 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 SIGMA KARSA MAGNA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MISONIX INC.Country of Origin
United States
Authorized Representative
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
Jan 27, 2024
Expiry Date
Oct 18, 2027
Product Type
Surgical Orthopaedic Equipment
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