RADIFOCUS Guide Wire M - Indonesia BPOM Medical Device Registration
RADIFOCUS Guide Wire M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501318233. The device is manufactured by TERUMO VIETNAM CO., LTD. from Vietnam, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO VIETNAM CO., LTD.Country of Origin
Vietnam
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Feb 08, 2023
Expiry Date
Nov 28, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
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