HANCOCK II Aortic Obturators - Indonesia BPOM Medical Device Registration
HANCOCK II Aortic Obturators is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10504714024. The device is manufactured by MEDTRONIC HEART VALVES DIVISION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDTRONIC HEART VALVES DIVISIONCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Jul 04, 2021
Expiry Date
Feb 13, 2026
Product Type
Surgical Cardiology Equipment
Cardiovascular surgical instruments.
Non Electromedic Non Sterile
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