OPTIMUS CMF System Cranioplasty plate - Indonesia BPOM Medical Device Registration
OPTIMUS CMF System Cranioplasty plate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003911213. The device is manufactured by OSTEONIC CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OSTEONIC CO., LTD.Country of Origin
Korea
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Jl. BSD Grand Boulevard, BSD Green Office Park, BSD City, Wing B, 3rd floor, Zone 7C
Registration Date
Aug 16, 2022
Expiry Date
May 31, 2024
Product Type
Therapeutic Neurology Equipment
Preformed alterable cranioplasty plate.
Non Electromedic Non Sterile
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OSTEONIC Optimus CMF System Cranioplasty Plate
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