ELLIQUENCE Surgi-Max Ultra - Indonesia BPOM Medical Device Registration
ELLIQUENCE Surgi-Max Ultra is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520076. The device is manufactured by ELLIQUENCE, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ELLIQUENCE, LLCCountry of Origin
United States
Authorized Representative
PT. MAIN MEDICAL SYNERGYAR Address
Jalan Gajah Mada No. 112 G-H
Registration Date
Feb 10, 2025
Expiry Date
Feb 12, 2029
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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