ULTRAPRO Hernia System - Indonesia BPOM Medical Device Registration
ULTRAPRO Hernia System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420031. The device is manufactured by JOHNSON & JOHNSON INTERNATIONAL from Belgium, 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
JOHNSON & JOHNSON INTERNATIONALCountry of Origin
Belgium
Authorized Representative
PT. JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
Mar 28, 2024
Expiry Date
May 17, 2028
Product Type
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