BAIDE External Fixation System - Indonesia BPOM Medical Device Registration
BAIDE External Fixation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302710567. The device is manufactured by JIANGSU BAIDE MEDICAL INSTRUMENTS 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 INSTRUMENTS 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
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