ULTRAPRO Mesh - Indonesia BPOM Medical Device Registration
ULTRAPRO Mesh is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420032. The device is manufactured by JOHNSON & JOHNSON MEDICAL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. 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 GMBH.Country of Origin
Germany
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
Apr 02, 2024
Expiry Date
May 17, 2028
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
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