Q-MASTER Q-Switched Nd:YAG System - Indonesia BPOM Medical Device Registration
Q-MASTER Q-Switched Nd:YAG System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603610355. The device is manufactured by AMI INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AMI INC.Country of Origin
Korea
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
JL. TANAH ABANG II NO. 37
Registration Date
Mar 22, 2020
Expiry Date
Jan 10, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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