BAIDE Titanium Bone Implant Screw - Indonesia BPOM Medical Device Registration
BAIDE Titanium Bone Implant Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302513824. The device is manufactured by JIANGSU BAIDE MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. YANTRA REKA SAKSANAMAS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JIANGSU BAIDE MEDICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. YANTRA REKA SAKSANAMASAR Address
Taman Palem Lestari Blok A3 No.38 Jl. Kamal raya Outering Road, Cengkareng Barat
Registration Date
Feb 04, 2019
Expiry Date
Dec 17, 2023
Product Type
Prosthetic Orthopedic Equipment
Single/multiple component metallic bone fixation appliances and accessories.
Non Electromedic Non Sterile
SOLAMED Laparatomy Sponges
SURGE INDUSTRIAL CO. LTD.
BAIDE Titanium Bone Implant Plates
JIANGSU BAIDE MEDICAL INSTRUMENTS CO., LTD.
BAIDE Large Fragment System
JIANGSU BAIDE MEDICAL INSTRUMENTS CO., LTD.
BAIDE Small Fragment System
JIANGSU BAIDE MEDICAL INSTRUMENTS CO., LTD.
BAIDE External Fixation System
JIANGSU BAIDE MEDICAL INSTRUMENTS CO., LTD.