Brand Name | SHILEY |
Type of Device | TUBE, TRACHEOSTOMY (W/WO CONNECTOR) |
Manufacturer (Section D) |
MMJ SA DE CV (USD) |
ave henequen no 1181 desarroll |
ciudad juarez 32590 |
MX 32590 |
|
Manufacturer (Section G) |
MMJ SA DE CV (USD) |
ave henequen no 1181 desarroll |
|
ciudad juarez 32590 |
MX
32590
|
|
Manufacturer Contact |
avi
kluger
|
5920 longbow drive |
boulder, CO 80301
|
3035306582
|
|
MDR Report Key | 9239671 |
MDR Text Key | 163796037 |
Report Number | 2936999-2019-00895 |
Device Sequence Number | 1 |
Product Code |
BTO
|
UDI-Device Identifier | 30884522006709 |
UDI-Public | 30884522006709 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K884730 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
10/25/2019 |
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 | 8PERC |
Device Catalogue Number | 8PERC |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
10/09/2019 |
Initial Date FDA Received | 10/25/2019 |
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 |