DRAGON CROWN Percutaneous Kyphoplasty System - Indonesia BPOM Medical Device Registration
DRAGON CROWN Percutaneous Kyphoplasty System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320697. The device is manufactured by DRAGON CROWN MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PATRIOT MEDIKA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DRAGON CROWN MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. PATRIOT MEDIKA NUSANTARAAR Address
Ruko Paramount Sparks, Blok B, No. 07, Jl. Raya Kelapa Dua
Registration Date
May 30, 2023
Expiry Date
Dec 31, 2024
Product Type
Prosthetic Orthopedic Equipment
Polymethylmethacrylate (PMMA) bone cement.
Non Electromedic Sterile
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