MEDTRONIC Ventricular Catheters - Indonesia BPOM Medical Device Registration
MEDTRONIC Ventricular Catheters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003022783. The device is manufactured by MEDTRONIC DOMINICANA (MANUFACTURA) S.A. from Dominican, 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 DOMINICANA (MANUFACTURA) S.A.Country of Origin
Dominican
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
May 17, 2020
Expiry Date
Mar 12, 2025
Product Type
Therapeutic Neurology Equipment
Central nervous system fluid shunt and components.
Non Electromedic Sterile
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MEDTRONIC CSF Valves And Buttons
MEDTRONIC Shunt Kits
MEDTRONIC Shunt Accessories
MEDTRONIC Lumboperitonial Shunt
MEDTRONIC Cardiac / Peritoneal Catheters
MEDTRONIC Ports And Reservoirs
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