MEDTRONIC RACT - Indonesia BPOM Medical Device Registration
MEDTRONIC RACT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207717574. The device is manufactured by MEDTRONIC PERFUSION SYSTEMS. from United States, 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
MEDTRONIC PERFUSION SYSTEMS.Country of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Sep 04, 2020
Expiry Date
Apr 11, 2024
Product Type
Haematology Package and Kit
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