Brand Name | 840 VENTILATOR |
Type of Device | VENTILATOR, CONTINUOUS, FACILITY USE |
Manufacturer (Section D) |
COVIDIEN |
micheal collins rd mervue |
galway |
|
Manufacturer (Section G) |
COVIDIEN |
micheal collins rd mervue |
|
galway |
|
Manufacturer Contact |
ray
maroofian
|
2101 faraday av |
carlsbad, CA 92008
|
7606035334
|
|
MDR Report Key | 6650705 |
MDR Text Key | 77869822 |
Report Number | 8020893-2017-06625 |
Device Sequence Number | 1 |
Product Code |
CBK
|
UDI-Device Identifier | 10884521077133 |
UDI-Public | 10884521077133 |
Combination Product (y/n) | N |
Reporter Country Code | IN |
PMA/PMN Number | K970460 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
foreign,health professional,o |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
05/30/2017 |
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 |
Health Professional
|
Device Model Number | 840 |
Device Catalogue Number | 840 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
05/30/2017 |
Initial Date FDA Received | 06/19/2017 |
Supplement Dates Manufacturer Received | 05/30/2017
|
Supplement Dates FDA Received | 09/07/2017
|
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 02/16/2011 |
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 |
|
|