St Jude Scs 3662 User Manual

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  1. St Jude Scs 3662 User Manual 2016
  2. St Jude Model 3662
  3. St Jude Scs 3662 User Manual Download
  4. St Jude Scs 3662 User Manual Instructions
  • CAUTION: These products are intended for use by or under the direction of a physician. Prior to use, reference the Instructions for Use, inside the product carton (when available) or online for more detailed information on Indications, Contraindications, Warnings, Precautions and Adverse Events.
  • MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION 3186 SCS LEAD.
  • The combination of Abbott and St. Jude Medical creates a medical device leader offering more breakthrough inventions and expertise across the areas of cardiovascular, diabetes and neuromodulation. Our solutions include spinal cord stimulation and dorsal root ganglion therapy for targeted pain syndromes and deep brain stimulation.
  • MRI Procedure Informatoni. Jude Medical MR Conditional Neurostimulation Systems. Clinician's Manual. Refer to the appropriate clinician’s manual or user’s guide for non -MRI related information. If you have any questions, contact. (Procam™ IPG Modes 3660 and 3662 only).
  • CAUTION: These products are intended for use by or under the direction of a physician. Prior to use, reference the Instructions for Use, inside the product carton (when available) or online for more detailed information on Indications, Contraindications, Warnings, Precautions and Adverse Events. Illustrations are artist's representations only and should not be considered as engineering.

Conflict of Interest and Source of Funding: Dr. Pintea has received support for travel, conference presentations, and training support from St. Jude Medical Inc. Kinfe works as a consultant for Medtronic Inc. Jude Medical Inc.For the remaining authors, none were declared. For more information on author guidelines, an explanation of our peer review process, and conflict of interest.

St Jude Scs 3662 User Manual 2016

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St Jude Model 3662


ST. JUDE MEDICAL - NEUROMODULATION 3186 SCS LEADBack to Search Results
Model Number 3186
Device Problem Adverse Event Without Identified Device or Use Problem
Event Date 01/01/2012
Event Type Injury
Event Description

Device 2 of 2. Reference mfr report # 1627487-2013-12664. It was reported the pt called in response to the charger swap program letter. The pt has not used the sys in several years due to the sys aggravating her parkinson's symptoms. Pt is contemplating a sys explant. Note: the pt has two leads from the same lot number.

Manufacturer Narrative

Sjm has limited information related to the patient's medical history and is unable to form an opinion as to the relevancy of the patient's history to the event reported. Sjm defers to the patient's physician regarding medical history. Jr x347 manual download.

Search Alerts/Recalls

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St Jude Scs 3662 User Manual Download


St Jude Scs 3662 User Manual Instructions

Type of DeviceSCS LEAD
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
connie timmons
6901 preston rd.
plano , TX 75024
9723098054
MDR Report Key3117606
Report Number1627487-2013-12665
Device Sequence Number1
Product CodeLGW
Report Source Manufacturer
Source TypeConsumer
Reporter Occupation NOT APPLICABLE
Type of ReportInitial
Report Date04/18/2013
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/13/2013
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device EXPIRATION Date02/01/2011
Device MODEL Number3186
Device LOT Number2751895
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No
Date Manufacturer Received04/18/2013
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Date Device Manufactured02/01/2009
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient TREATMENT DATA
Date Received: 05/13/2013 Patient Sequence Number: 1