SPIDERFX Embolic Protection Device - Indonesia BPOM Medical Device Registration
SPIDERFX Embolic Protection Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501718400. The device is manufactured by EV3 INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EV3 INC.Country of Origin
United States
Authorized Representative
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
Sep 19, 2024
Expiry Date
Feb 20, 2029
Product Type
Diagnostic Cardiology Equipment
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