Brand Name | UNKNOWN_MEDICAL_PRODUCT |
Type of Device | STRECHER, WHEELED |
Manufacturer (Section D) |
STRYKER MEDICAL-KALAMAZOO |
3800 east centre avenue |
portage MI 49002 |
|
Manufacturer (Section G) |
STRYKER MEDICAL-KALAMAZOO |
3800 east centre avenue |
|
portage MI 49002 |
|
Manufacturer Contact |
brandon
luckas
|
3800 east centre avenue |
portage, MI 49002
|
2693292100
|
|
MDR Report Key | 18981031 |
MDR Text Key | 338628737 |
Report Number | 0001831750-2024-00336 |
Device Sequence Number | 1 |
Product Code |
FPO
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
User Facility |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
05/08/2024 |
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? |
Yes
|
Device Catalogue Number | UNK_MED |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
02/29/2024
|
Initial Date FDA Received | 03/26/2024 |
Supplement Dates Manufacturer Received | 02/29/2024
|
Supplement Dates FDA Received | 05/08/2024
|
Was Device Evaluated by Manufacturer? |
No
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
|
|
|