Brand Name | JWALKER BOOT |
Type of Device | JWALKER BOOT |
Manufacturer (Section D) |
BREG, INC |
2885 loker ave east |
carlsbad CA 92010 |
|
Manufacturer (Section G) |
BREG, INC |
2885 loker avenue east |
|
carlsbad CA 92010 |
|
Manufacturer Contact |
carol
emerson
|
2885 loker avenue east |
carlsbad, CA 92010
|
7607955823
|
|
MDR Report Key | 7047204 |
MDR Text Key | 93168140 |
Report Number | 2028253-2017-00080 |
Device Sequence Number | 1 |
Product Code |
IQI
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
distributor |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
11/17/2017 |
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 |
Lay User/Patient
|
Device Model Number | BL210007 |
Device Catalogue Number | BL210007 |
Is the Reporter a Health Professional? |
No
|
Was the Report Sent to FDA? |
No
|
Initial Date Manufacturer Received |
10/27/2017 |
Initial Date FDA Received | 11/20/2017 |
Was Device Evaluated by Manufacturer? |
No
|
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 |
|
|