Brand Name | MECHANICAL (MANUAL) WHEELCHAIR |
Type of Device | WHEELCHAIR |
Manufacturer (Section D) |
TAIWAN AN I CO.,LTD. |
no.1 been ting been-tsuoh |
village, shi-koou shiang |
chia-yi shiann |
TW |
|
Manufacturer (Section G) |
A & I INDUSTRIES LTD |
lian du industry park |
le liu town, shunde dist. |
foshan city, guangdong |
TW
|
|
Manufacturer Contact |
kevin
walls
|
33 golden eagle lane |
|
littleton, CO 80127
|
7209625412
|
|
MDR Report Key | 6199796 |
MDR Text Key | 63638708 |
Report Number | 9612393-2014-00019 |
Device Sequence Number | 1 |
Product Code |
IOR
|
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 |
02/24/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/28/2014 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Lay User/Patient
|
Device Model Number | IN88AHANFRFF |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 02/24/2014 |
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 |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
|
|
|