Brand Name | STERIS RAPTOR GRASPING DEVICE |
Type of Device | ENDOSCOPIC GRASPING/CUTTING INSTRUMENT, NON-POWERED |
Manufacturer (Section D) |
US ENDOSCOPY / UNITED STATES ENDOSCOPY GROUP, INC. |
mentor OH 44060 |
|
MDR Report Key | 13734237 |
MDR Text Key | 287247722 |
Report Number | MW5108030 |
Device Sequence Number | 1 |
Product Code |
OCZ
|
UDI-Device Identifier | 00724995183653 |
UDI-Public | (01)00724995183653 |
Combination Product (y/n) | Y |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
03/08/2022 |
2 Devices were Involved in the Event: |
1
2
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/10/2022 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 00711177 |
Device Catalogue Number | 00711177 |
Device Lot Number | 2200981 |
Is the Reporter a Health Professional? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
|
|