Brand Name | ZIO AT PATCH |
Type of Device | DETECTOR AND ALARM, ARRHYTHMIA |
Manufacturer (Section D) |
IRHYTHM TECHNOLOGIES, INC |
699 8th st suite 600 |
san francisco CA 94103 |
|
Manufacturer (Section G) |
IRHYTHM TECHNOLOGIES, INC |
11085 knott avenue suite b |
|
cypress CA 90630 |
|
Manufacturer Contact |
mazi
kiani
|
699 8th st suite 600 |
san francisco, CA 94103
|
9494132147
|
|
MDR Report Key | 12807158 |
MDR Text Key | 281670234 |
Report Number | 3007208829-2021-00130 |
Device Sequence Number | 1 |
Product Code |
DSI
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K163512 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Consumer,Company Representative |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
11/10/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 11/12/2021 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Expiration Date | 03/13/2022 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 10/25/2021 |
Date Manufacturer Received | 11/10/2021 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 09/14/2021 |
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;
|
Patient Age | 32 YR |
Patient Sex | Female |