MEDTRONIC CSF-Unitized Shunts - Indonesia BPOM Medical Device Registration
MEDTRONIC CSF-Unitized Shunts is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003611540. The device is manufactured by MEDTRONIC NEUROSURGERY 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 NEUROSURGERYCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Nov 19, 2019
Expiry Date
Apr 11, 2024
Product Type
Therapeutic Neurology Equipment
Central nervous system fluid shunt and components.
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