Brand Name | FLEXCATH ADVANCE STEERABLE SHEATH |
Type of Device | CATHETER, STEERABLE |
Manufacturer (Section D) |
MEDTRONIC CRYOCATH LP |
16771 chemin ste-marie |
kirkland,qc H9H 5 H3 |
CA H9H 5H3 |
|
Manufacturer (Section G) |
MEDTRONIC CRYOCATH LP |
16771 chemin ste-marie |
|
kirkland,qc H9H 5 H3 |
CA
H9H 5H3
|
|
Manufacturer Contact |
voula
radiotis
|
16771 chemin ste-marie |
kirkland,qc H9H 5-H3
|
CA
H9H 5H3
|
5146941212
|
|
MDR Report Key | 4413834 |
MDR Text Key | 17291812 |
Report Number | 3002648230-2015-00009 |
Device Sequence Number | 1 |
Product Code |
DRA
|
Combination Product (y/n) | N |
Reporter Country Code | JA |
PMA/PMN Number | K123591 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,Company Representative,company representati |
Reporter Occupation |
Physician
|
Type of Report
| Initial,Followup |
Report Date |
12/18/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | 4FC12 |
Device Catalogue Number | 4FC12 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
12/18/2014
|
Initial Date FDA Received | 01/13/2015 |
Supplement Dates Manufacturer Received | 12/18/2014
|
Supplement Dates FDA Received | 09/15/2017
|
Was Device Evaluated by Manufacturer? |
No
|
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 Outcome(s) |
Other;
|
|
|