OMNIPORE Surgical Implants - Indonesia BPOM Medical Device Registration
OMNIPORE Surgical Implants is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602024966. The device is manufactured by MATRIX SURGICAL USA from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ORIONTAMA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MATRIX SURGICAL USACountry of Origin
United States
Authorized Representative
PT. ORIONTAMA JAYAAR Address
Jl. Sutomo No. 122
Registration Date
Sep 02, 2020
Expiry Date
Feb 21, 2025
Product Type
Prosthetic Surgical Equipment
Polytetrafluoroethylene with carbon fibers composite implant material.
Non Electromedic Sterile
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