FINECROSS MG Coronary Micro Guide Catheter - Indonesia BPOM Medical Device Registration
FINECROSS MG Coronary Micro Guide Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501900123. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY OF TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
May 27, 2023
Expiry Date
Jan 06, 2027
Product Type
Diagnostic Cardiology Equipment
Continuous flush catheter.
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