EZ STEER DS Electrophysiology Catheter - Indonesia BPOM Medical Device Registration
EZ STEER DS Electrophysiology Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501703853. 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 PT. JOHNSON & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSENSE WEBSTER, INC.Country of Origin
Mexico
Authorized Representative
PT. JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Dec 01, 2020
Expiry Date
Sep 02, 2025
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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