MEDTRONIC Patient Connector - Indonesia BPOM Medical Device Registration
MEDTRONIC Patient Connector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501913937. The device is manufactured by PLEXUS MANUFACTURING SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PLEXUS MANUFACTURING SDN. BHD.Country of Origin
Malaysia
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 19, 2024
Expiry Date
Feb 07, 2028
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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