AnyPlusII Pedicle Screw System-3 - Indonesia BPOM Medical Device Registration
AnyPlusII Pedicle Screw System-3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420360. 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., LTD.Country of Origin
Korea
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Sep 20, 2024
Expiry Date
Jul 13, 2026
Product Type
Prosthetic Orthopedic Equipment
Spinal interlaminal fixation orthosis.
Non Electromedic Non Sterile
AnyPlusII Pedicle Screw System-6
AnyPlus II Pedicle Screw System-7
AnyPlusII Pedicle Screw System-5
AnyPlusII Pedicle Screw System-4
AnyPlusII Pedicle Screw System-2
AnyPlusII Pedicle Screw System-1
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AnyPlusII Pedicle Screw System-6
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