PROCEED Ventral Patch - Indonesia BPOM Medical Device Registration
PROCEED Ventral Patch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602110225. 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 & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOHNSON & JOHNSON MEDICAL GMBHCountry of Origin
Germany
Authorized Representative
JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Sep 10, 2021
Expiry Date
Jul 23, 2026
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
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