Brand Name | ARROW SPRING WIRE GUIDE COMPONENT |
Type of Device | CATHETER HEMODIALYSIS IMPLANTE |
Manufacturer (Section D) |
ARROW INTERNATIONAL LLC |
morrisville NC |
|
Manufacturer (Section G) |
ARROW INTERNATIONAL DE MEXICO S.A. DE C.V. |
ave. washington 3701 |
colonia panamericana, chihuahua |
chihuahua 31200 |
MX
31200
|
|
Manufacturer Contact |
katharine
tarpley
|
3015 carrington mill blvd |
morrisville, NC 27560
|
|
MDR Report Key | 17593736 |
MDR Text Key | 321650117 |
Report Number | 9680794-2023-00584 |
Device Sequence Number | 1 |
Product Code |
MPB
|
Combination Product (y/n) | N |
Reporter Country Code | TW |
PMA/PMN Number | K993933 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,User Facility,Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
07/24/2023 |
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 |
Health Professional
|
Device Catalogue Number | AW-04435 |
Device Lot Number | 14F22G0223 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
07/24/2023
|
Initial Date FDA Received | 08/22/2023 |
Supplement Dates Manufacturer Received | 09/12/2023
|
Supplement Dates FDA Received | 09/13/2023
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 08/01/2022 |
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 |
Treatment | NOT REPORTED; NOT REPORTED |