Brand Name | PULSAR-18 T3 4/30/135 |
Type of Device | STENT, SUPERFICIAL FEMORAL ARTERY |
Manufacturer (Section D) |
BIOTRONIK AG, BUELACH, SWITZERLAND |
ackerstrasse 6 |
buelach CH-81 80 |
CH CH-8180 |
|
Manufacturer Contact |
|
6024 jean road |
lake oswego, OR 97035
|
8772459800
|
|
MDR Report Key | 18960710 |
MDR Text Key | 338760217 |
Report Number | 1028232-2024-01601 |
Device Sequence Number | 1 |
Product Code |
NIP
|
UDI-Device Identifier | 07640130446762 |
UDI-Public | (01)07640130446762(17)2502 |
Combination Product (y/n) | N |
Reporter Country Code | CH |
PMA/PMN Number | P160025 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Foreign,User Facility,Company Representative |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
04/16/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/22/2024 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 430478 |
Device Catalogue Number | SEE MODEL NO. |
Device Lot Number | 02220959 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 04/16/2024 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 02/16/2022 |
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 |
|
|