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Step 1. Patient Information

Step 2. Implant Physician Information

Step 3. Following/Attending Physician Information

Step 4. Device(s) Information

Step 5. Review and Submit Registration

  -Review and confirm this registration.
  -When registration confirmation is returned, print a copy for your records

 

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Review and Confirmation
Review the information for this registration.
Items marked in yellow are incomplete.

Patient: LastName, FirstName  
Last Name   First Name Initial
 
Patient Chart Number   Sex Date of Birth
  M F
Social Security Number    
- -      

    Patient Expired

Address Line 1   Patient Telephone Number
Address Line 2
  ( )
City   State/Province   Postal Code
   
Country      
     
 

Implant Physician  
Last Name   First Name   MI
   
M.D.    D.O.      
First Specialty   Second Specialty
 

Telephone Number   Fax Number
( )   ( )
Address Line 1  
   
Address Line 2  
   
Address Line 3  
   
City   State/Province   Postal Code
   
 

Following/Attending Physician  
Last Name   First Name   MI
   
M.D.    D.O.      
First Specialty   Second Specialty
 

Telephone Number   Fax Number
( )   ( )
Address Line 1  
   
Address Line 2  
   
Address Line 3  
   
City   State/Province   Postal Code
   
 


Insertable Loop Recorder {Serial/Lot Number}  
Model Number   Serial/Lot Number     Implant Date
{Filled in by server}   {Filled in by server}      
/
/
Manufacturer        
  {Product Family -Medtronic Only}

Diagnostic Reason for Monitoring    
Syncope
Presyncope
Dizziness
 
Palpitations
Seizures
Other

Implant Position
Patient Activated
Pectoral    Left Right
Submammary    Left Right
Subaxillary    Left Right
Other
 
Auto Activated
Recommended left implant site
Other

Parameter Settings (Fill out areas that apply to this implant)
Memory Settings
21 Min. 42 Min.
   

Patient Activated Events / Auto Activated Events
1 / none    
3 / none    
1 / 13/14    
3 / 5/6    
 
Record
First Last Occuring Events
   
Gain
X1   X2   X4   X8  

Sensitivity
1   2   3   4   5  
6   7   8   9   10  
11   12   13   14   15  
 

Hemodynamic Monitor {Serial/Lot Number}  
Model Number   Serial/Lot Number     Implant Date
{Filled in by server}   {Filled in by server}      
/
/
Manufacturer        
  {Product Family -Medtronic Only}

Previous Device Data
Model Number   Serial/Lot Number
 
Device Manufacturer
 
  Prior Implant Date
   
/
/
 

Pressure Sensing Lead {Serial/Lot Number}  
Model Number   Serial/Lot Number     Implant Date
{Filled in by server}   {Filled in by server}      
/
/
Manufacturer        
  {Product Family -Medtronic Only}

Previous Device Data
Model Number   Serial/Lot Number
 
Device Manufacturer
 
  Prior Implant Date
   
/
/
 


The information above marked in yellow is not required for registration.

To complete this registration, press the confirm button below.

Medtronic.com will then display a printable version of the registration received. Please print this for your records.

 
 

 

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