Brand Name | TITAN TOUCH |
Type of Device | INFLATABLE PENILE PROSTHESIS |
Manufacturer (Section D) |
COLOPLAST A/S |
holtedam 1 |
humlebaek, 3050 |
DA 3050 |
|
Manufacturer (Section G) |
COLOPLAST MANUFACTURING US, LLC |
1601 west river road north |
|
minneapolis, mn |
|
Manufacturer Contact |
stephanie
perryman
|
1601 west river road north |
minneapolis, mn
|
|
MDR Report Key | 9846972 |
MDR Text Key | 183876129 |
Report Number | 2125050-2020-00245 |
Device Sequence Number | 1 |
Product Code |
FHW
|
UDI-Device Identifier | 05708932539197 |
UDI-Public | 05708932539197 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P000006 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
03/16/2020 |
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 |
Lay User/Patient
|
Device Model Number | ES29202400 |
Device Catalogue Number | ES2920 |
Device Lot Number | 5408952 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
02/17/2020 |
Initial Date FDA Received | 03/18/2020 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Hospitalization;
Required Intervention;
|
Patient Age | 73 YR |