Brand Name | ARROW ARROW CATH-LAB SHEATH INTRO SET |
Type of Device | CATHETER, PERCUTANEOUS |
Manufacturer (Section D) |
ARROW INTERNATIONAL INC. |
reading PA |
|
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
|
9194334854
|
|
MDR Report Key | 6965032 |
MDR Text Key | 89841075 |
Report Number | 9680794-2017-00222 |
Device Sequence Number | 1 |
Product Code |
DQY
|
Combination Product (y/n) | N |
Reporter Country Code | KS |
PMA/PMN Number | K862056 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
distributor,foreign,health pr |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
10/11/2017 |
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 Expiration Date | 01/31/2021 |
Device Catalogue Number | CL-07524 |
Device Lot Number | 14F16B0198 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 11/06/2017 |
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
10/11/2017 |
Initial Date FDA Received | 10/20/2017 |
Supplement Dates Manufacturer Received | 11/29/2017
|
Supplement Dates FDA Received | 11/29/2017
|
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 02/22/2016 |
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 |
|
|