ARTFX Trauma Implant (II) - Indonesia BPOM Medical Device Registration
ARTFX Trauma Implant (II) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320747. 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 TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARTFX MEDICAL LLCCountry of Origin
United States
Authorized Representative
TRITRA PRIMA INDONESIAAR Address
Central Park Cikarang Blok A1 No. 02
Registration Date
Jul 03, 2023
Expiry Date
May 22, 2027
Product Type
Prosthetic Orthopedic Equipment
Single/multiple component metallic bone fixation appliances and accessories.
Non Electromedic Non Sterile
ARTFX Trauma Instrument
ARTFX Trauma Implant (III)
ARTFX Trauma Implant (IV)
ARTFX Spine Instruments
ARTFX Spondylolisthesis Spinal Fixation (3)
ARTFX Spondylolisthesis Spinal Fixation (2)
ARTFX Spondylolisthesis Spinal Fixation (1)
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