ARTFX Spine Instruments - Indonesia BPOM Medical Device Registration
ARTFX Spine Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303220308. The device is manufactured by ARTFX MEDICAL LLC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ARTFX MEDICAL LLCCountry of Origin
United States
Authorized Representative
TRITRA PRIMA INDONESIAAR Address
Taman Sari Persada Blok F-1 Nomor 10
Registration Date
Dec 30, 2022
Expiry Date
May 22, 2027
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
ARTFX Trauma Instrument
ARTFX Trauma Implant (II)
ARTFX Trauma Implant (III)
ARTFX Trauma Implant (IV)
ARTFX Spondylolisthesis Spinal Fixation (3)
ARTFX Spondylolisthesis Spinal Fixation (2)
ARTFX Spondylolisthesis Spinal Fixation (1)
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