Brand Name | REVO MRI SURESCAN |
Type of Device | PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE |
Manufacturer (Section D) |
MEDTRONIC MED REL MEDTRONIC PUERTO RICO |
road 31, km. 24, hm 4 |
ceiba norte industrial park |
juncos PR 00777 |
|
Manufacturer (Section G) |
MEDTRONIC MED REL MEDTRONIC PUERTO RICO |
road 31, km. 24, hm 4 |
ceiba norte industrial park |
juncos PR 00777 |
|
Manufacturer Contact |
paula
bixby
|
8200 coral sea st ne |
mounds view, MN 55112
|
7635055378
|
|
MDR Report Key | 9346079 |
MDR Text Key | 182626486 |
Report Number | 3004209178-2019-22165 |
Device Sequence Number | 1 |
Product Code |
LWP
|
UDI-Device Identifier | 00613994614742 |
UDI-Public | 00613994614742 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P090013 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
12/06/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Lay User/Patient
|
Device Expiration Date | 03/14/2013 |
Device Model Number | RVDR01 |
Device Catalogue Number | RVDR01 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
10/24/2019 |
Initial Date FDA Received | 11/20/2019 |
Supplement Dates Manufacturer Received | 11/20/2019
|
Supplement Dates FDA Received | 12/06/2019
|
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 09/14/2011 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Patient Age | 76 YR |
|
|