AVIGO Hydrophilic Guidewire - Indonesia BPOM Medical Device Registration
AVIGO Hydrophilic Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501716669. 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
Registration Date
Feb 10, 2021
Expiry Date
Jan 13, 2026
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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