ARIX System Bone Screw - Indonesia BPOM Medical Device Registration
ARIX System Bone Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302717946. The device is manufactured by JEIL MEDICAL CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEIL MEDICAL CORPORATIONCountry of Origin
Korea
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Aug 06, 2024
Expiry Date
Jul 04, 2029
Product Type
Prosthetic Orthopedic Equipment
Smooth or threaded metallic bone fixation fastener.
Non Electromedic Non Sterile
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