ARTFX Spondylolisthesis Spinal Fixation (1) - Indonesia BPOM Medical Device Registration
ARTFX Spondylolisthesis Spinal Fixation (1) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302220322. The device is manufactured by ARTFX MEDICAL LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARTFX MEDICAL LLCCountry of Origin
United States
Authorized Representative
PT. TRITRA PRIMA INDONESIAAR Address
Taman Sari Persada Blok F-1 Nomor 10
Registration Date
Aug 31, 2022
Expiry Date
May 23, 2027
Product Type
Prosthetic Orthopedic Equipment
Pedicle screw spinal system
Non Electromedic Sterile
ARTFX Trauma Instrument
ARTFX Trauma Implant (II)
ARTFX Trauma Implant (III)
ARTFX Trauma Implant (IV)
ARTFX Spine Instruments
ARTFX Spondylolisthesis Spinal Fixation (3)
ARTFX Spondylolisthesis Spinal Fixation (2)
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