PROCEED Surgical Mesh - Indonesia BPOM Medical Device Registration
PROCEED Surgical Mesh is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420056. 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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
JOHNSON & JOHNSON MEDICAL GMBHCountry of Origin
Germany
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
May 25, 2024
Expiry Date
Feb 22, 2029
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
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