ENDURANT ™ IIs Stent Graft System - Indonesia BPOM Medical Device Registration
ENDURANT ™ IIs Stent Graft System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503420036. The device is manufactured by MEDTRONIC IRELAND from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDTRONIC IRELANDCountry of Origin
Ireland
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
Mar 06, 2024
Expiry Date
Feb 07, 2028
Product Type
Prosthetic Cardiology Equipment
Coronary stent
Non Electromedic Sterile
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