NAVISTAR Electrophysiology Catheter - Indonesia BPOM Medical Device Registration
NAVISTAR Electrophysiology Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420199. The device is manufactured by BIOSENSE WEBSTER, INC. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSENSE WEBSTER, INC.Country of Origin
Mexico
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
Apr 01, 2024
Expiry Date
Jan 25, 2029
Product Type
Diagnostic Cardiology Equipment
Electrode recording catheter or electrode recording probe.
Non Electromedic Sterile
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