Brand Name | DRIVE |
Type of Device | ROLLATOR |
Manufacturer (Section D) |
A & I INDUSTRIES LTD |
lian du industry park |
le liu town, shunde district |
foshan city, guangdong |
CH |
|
Manufacturer (Section G) |
A & I INDUSTRIES LTD |
lian du industry park |
le liu town, shunde district |
foshan city, guangdong |
CH
|
|
Manufacturer Contact |
kevin
walls
|
33 golden eagle lane |
littleton, CO 80127
|
7209625412
|
|
MDR Report Key | 17981882 |
MDR Text Key | 326234713 |
Report Number | 3004034546-2023-00002 |
Device Sequence Number | 1 |
Product Code |
ITJ
|
UDI-Device Identifier | 00822383972497 |
UDI-Public | 822383972497 |
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 |
10/21/2023 |
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 |
Lay User/Patient
|
Device Model Number | RTL10266DT |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 10/21/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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) |
Hospitalization;
|
Patient Sex | Female |
|
|