Brand Name | SINGLE RELEASE ADULT WALKER 9153629378 |
Type of Device | WALKER, MECHANICAL |
Manufacturer (Section D) |
GENTEEL HOMECARE PRODUCTS |
liyu industry area |
danzao nanhai foshan 5282 16 |
CH 528216 |
|
MDR Report Key | 4486576 |
MDR Text Key | 5563184 |
Report Number | 1531186-2015-00797 |
Device Sequence Number | 1 |
Product Code |
ITJ
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Distributor
|
Source Type |
Invalid Data |
Reporter Occupation |
Medical Equipment Company Technician/Representative
|
Type of Report
| Initial |
Report Date |
02/04/2015,01/29/2015 |
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 | 6281-A |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 02/04/2015 |
Distributor Facility Aware Date | 01/29/2015 |
Device Age | 1 YR |
Date Report to Manufacturer | 02/04/2015 |
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 02/05/2015 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
|
|
|