MARVEL Guidewire - Indonesia BPOM Medical Device Registration
MARVEL Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501815236. The device is manufactured by FMD CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FMD CO., LTD.Country of Origin
Japan
Authorized Representative
PT. BOSTON SCIENTIFIC INDONESIAAR Address
Prudential Tower lantai 28 Jl. Jend. Sudirman Kav. 79
Registration Date
Jul 22, 2022
Expiry Date
Apr 20, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
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