MEDTRONIC Bio Console 560 - Indonesia BPOM Medical Device Registration
MEDTRONIC Bio Console 560 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504022766. The device is manufactured by MEDTRONIC PERFUSION SYSTEMS from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDTRONIC PERFUSION SYSTEMSCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Oct 05, 2020
Expiry Date
Mar 12, 2025
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass pump speed control.
Non Radiation Electromedics
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