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The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s).
Please note that the intended use of a product may vary depending on geographical approvals.
See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.
For an MRI compatible device(s), consult the MRI information in the device manual(s) before performing an MRI.
If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.
Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.
Medtronic products placed on European markets bear the CE mark and the UKCA mark, if applicable.
For any further information, contact your local Medtronic representative and/or consult the Medtronic website at cema.medtronic.com.
Manufactured in Medtronic Puerto Rico (Juncos Prod. Center) Ceiba Norte Industrial Park Rd. 31 KM 24, HM4 00777 Juncos, Puerto Rico.