Cobalt™ XT VR MRI SureScan™ - Indonesia BPOM Medical Device Registration
Cobalt™ XT VR MRI SureScan™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503129030. The device is manufactured by MEDTRONIC EUROPE S.A.R.L from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDTRONIC EUROPE S.A.R.LCountry of Origin
Switzerland
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Dec 31, 2021
Expiry Date
Jan 13, 2026
Product Type
Prosthetic Cardiology Equipment
Implantable pacemaker pulse generator.
Non Radiation Electromedics
CROME™ VR MRI SureScan™
CROME™ DR MRI SureScan™
CROME™ VR MRI SureScan™
CROME™ HF CRT-D MRI SureScan™
CROME™ HF CRT-D MRI SureScan™
CROME™ HF Quad CRT-D MRI SureScan™
CROME™ DR MRI SureScan™
CROME™ HF Quad CRT-D MRI SureScan™
Cobalt™ XT DR MRI SureScan™
COBALT™ HF CRT-D MRI SureScan™
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