CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH - Indonesia BPOM Medical Device Registration
CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420053. The device is manufactured by FREUDENBERG MEDICAL LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FREUDENBERG MEDICAL LLC.Country of Origin
United States
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950
Registration Date
Jan 30, 2024
Expiry Date
Dec 08, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter introducer
Non Electromedic Sterile
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