ANYPLUS PEEK Cage System Instrument (TLIF) - Indonesia BPOM Medical Device Registration
ANYPLUS PEEK Cage System Instrument (TLIF) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303025078. The device is manufactured by GS MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GS MEDICAL CO., LTD.Country of Origin
Korea
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Jul 25, 2024
Expiry Date
Jul 13, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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