ADROIT ™ Guiding Catheter - Indonesia BPOM Medical Device Registration
ADROIT ™ Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320865. The device is manufactured by CARDINAL HEALTH MEXICO 244 S DE RL DE CV from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WEGO MEDIKA INDONESIA.
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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. WEGO MEDIKA INDONESIAAR Address
Jl. Tanah Abang II No.67 Kel. Petojo Selatan, Kec. Gambir, Jakarta Pusat
Registration Date
Nov 11, 2024
Expiry Date
May 01, 2028
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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