RADIFOCUS Guide Wire GT with Gold Coil - Indonesia BPOM Medical Device Registration
RADIFOCUS Guide Wire GT with Gold Coil is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220017. 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 TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY OF TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Mar 01, 2022
Expiry Date
Sep 07, 2026
Product Type
Diagnostic Cardiology Equipment
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