PRIMO MRI™ DR SureScan™ - Indonesia BPOM Medical Device Registration
PRIMO MRI™ DR SureScan™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503815655. 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 PT. MEDTRONIC INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDTRONIC EUROPE S.A.R.L.Country of Origin
Switzerland
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
Apr 07, 2024
Expiry Date
Feb 07, 2028
Product Type
Prosthetic Cardiology Equipment
Implantable pacemaker pulse generator.
Non Radiation Electromedics
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PRIMO MRI™ DR SureScan™
PRIMO MRI™ VR SureScan™
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