MAXMORE Spine Stenosis Intralaminar Endoscopy System - Indonesia BPOM Medical Device Registration
MAXMORE Spine Stenosis Intralaminar Endoscopy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21301021489. The device is manufactured by HOOGLAND SPINE PRODUCTS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HOOGLAND SPINE PRODUCTS GMBHCountry of Origin
Germany
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Foresta Business Loft 6 Unit 2 BSD City, Jl. BSD Boulevard Utara, Kode Pos 15331
Registration Date
Jan 20, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Orthopedic Equipment
Arthroscope
Non Electromedic Non Sterile
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