OSTEONIC Optimus CMF System Instrument - Indonesia BPOM Medical Device Registration
OSTEONIC Optimus CMF System Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420305. The device is manufactured by OSTEONIC CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
OSTEONIC CO., LTD.Country of Origin
Korea
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Foresta Business Loft 6 Unit 2, Jl. BSD Boulevard Utara, Kelurahan Lengkong Kulon, Kecamatan Pagedangan, Kabupaten Tangerang, Banten 15331, Indonesia
Registration Date
Nov 20, 2024
Expiry Date
Feb 19, 2029
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
OSTEONIC Optimus CMF System Fixation Screw
OSTEONIC Optimus CMF System Fixation Plate
OSTEONIC Optimus CMF System Cranioplasty Plate
OPTIMUS CMF System B
OPTIMUS CMF System Cranioplasty plate
OPTIMUS CMF System Fixation Screw
OPTIMUS CMF System
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