Brand Name | UNKNOWN_INSTRUMENTS_PRODUCT |
Type of Device | UNKNOWN |
Manufacturer (Section D) |
STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP |
1941 stryker way |
portage MI 49002 |
|
Manufacturer (Section G) |
STRYKER INSTRUMENTS-PUERTO RICO |
las palmas industrial park |
highway #3, km 130.2 |
arroyo 00615 |
*
00615
|
|
Manufacturer Contact |
zach
baker
|
1941 stryker way |
portage, MI 49002
|
2693237700
|
|
MDR Report Key | 12845153 |
MDR Text Key | 281139354 |
Report Number | 3015967359-2021-02604 |
Device Sequence Number | 1 |
Product Code |
DZA
|
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 |
02/03/2022 |
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? |
No
|
Device Operator |
Health Professional
|
Device Catalogue Number | UNK_INS |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
10/22/2021
|
Initial Date FDA Received | 11/19/2021 |
Supplement Dates Manufacturer Received | 02/02/2022
|
Supplement Dates FDA Received | 02/03/2022
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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 |
Patient Outcome(s) |
Required Intervention;
Other;
|