Actis Duofix Hip Prosthesis - Indonesia BPOM Medical Device Registration
Actis Duofix Hip Prosthesis is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420322. The device is manufactured by JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.Country of Origin
China
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
Aug 30, 2024
Expiry Date
Feb 21, 2028
Product Type
Prosthetic Orthopedic Equipment
Hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis.
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