Brand Name | SMARTLIFE LARGE ASPETIC HOUSING |
Type of Device | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Manufacturer (Section D) |
STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP |
1941 stryker way |
portage MI 49002 |
|
Manufacturer (Section G) |
STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP |
1941 stryker way |
|
portage MI 49002 |
|
Manufacturer Contact |
zach
baker
|
1941 stryker way |
portage, MI 49002
|
2693237700
|
|
MDR Report Key | 12699089 |
MDR Text Key | 278411117 |
Report Number | 3015967359-2021-02398 |
Device Sequence Number | 1 |
Product Code |
HWE
|
UDI-Device Identifier | 07613327128819 |
UDI-Public | 07613327128819 |
Combination Product (y/n) | N |
Reporter Country Code | FR |
PMA/PMN Number | EXEMPT |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
10/26/2021 |
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 Model Number | 7126-120-000 |
Device Catalogue Number | 7126120000 |
Device Lot Number | 19158 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
10/22/2021 |
Initial Date FDA Received | 10/26/2021 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 06/07/2019 |
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 |