REFLECT Scoliosis Correction System - Indonesia BPOM Medical Device Registration
REFLECT Scoliosis Correction System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420076. The device is manufactured by GLOBUS MEDICAL, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GLOBUS MEDICAL, INC.Country of Origin
United States
Authorized Representative
PT. ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Apr 03, 2024
Expiry Date
Jan 08, 2025
Product Type
Prosthetic Orthopedic Equipment
Spinal intervertebral body fixation orthosis.
Non Electromedic Sterile
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