PREFACE Guiding Sheath - Indonesia BPOM Medical Device Registration
PREFACE Guiding Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420182. The device is manufactured by CARDINAL HEALTH MEXICO 244 S DE RL DE CV from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARDINAL HEALTH MEXICO 244 S DE RL DE CVCountry of Origin
Mexico
Authorized Representative
PT. JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan
Registration Date
Sep 26, 2024
Expiry Date
Jan 25, 2029
Product Type
Diagnostic Cardiology Equipment
Catheter introducer.
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