MEGAFIX Spinal Internal Fixation System, Intervertebral Body - Indonesia BPOM Medical Device Registration
MEGAFIX Spinal Internal Fixation System, Intervertebral Body is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320572. The device is manufactured by SEOHANCARE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SKBIO NUSA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEOHANCARE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. SKBIO NUSA MEDICAAR Address
Komplek Wijaya Graha Puri Blok G/17, Jl. Wijaya 2 RT.008 / RW.001
Registration Date
Dec 13, 2024
Expiry Date
Sep 21, 2027
Product Type
Prosthetic Orthopedic Equipment
Thoracolumbosacral pedicle screw system
Non Electromedic Non Sterile
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