PROLENE Polypropylene Mesh - Indonesia BPOM Medical Device Registration
PROLENE Polypropylene Mesh is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420061. The device is manufactured by ETHICON, LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ETHICON, LLC.Country of Origin
United States
Authorized Representative
PT. JOHNSON AND JOHNSON INDONESIA TWOAR Address
Revenue Tower, Lt.27 District 8, SCBD Lot 13 Jl. Jenderal Sudirman Kav. 52-53 Jakarta 12190, Indonesia
Registration Date
Jan 04, 2025
Expiry Date
Jan 26, 2028
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
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