PYXIS 3D Titanium PLIF Cage (Sterile) - Indonesia BPOM Medical Device Registration
PYXIS 3D Titanium PLIF Cage (Sterile) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320855. The device is manufactured by GS MEDICAL CO., LTD 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
GS MEDICAL CO., LTDCountry of Origin
Korea
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Jul 02, 2024
Expiry Date
Jul 13, 2026
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Sterile
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