HYPERFORM Occlusion Balloon System - Indonesia BPOM Medical Device Registration
HYPERFORM Occlusion Balloon System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504717906. The device is manufactured by MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
May 18, 2022
Expiry Date
Feb 16, 2027
Product Type
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