MIRAGE ™ .008 Hydrophilic Guidewire - Indonesia BPOM Medical Device Registration
MIRAGE ™ .008 Hydrophilic Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501716668. The device is manufactured by MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULARCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama
Registration Date
Jan 12, 2025
Expiry Date
Feb 20, 2029
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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