Brand Name | EXPECT PULMONARY OLYMPUS 25GA |
Type of Device | ENDOBRONCHIAL ULTRASOUND TRANSBRONCHIAL ASPIRATION NEEDLE |
Manufacturer (Section D) |
BOSTON SCIENTIFIC - SPENCER |
780 brookside drive |
spencer IN 47460 |
|
Manufacturer (Section G) |
BOSTON SCIENTIFIC - SPENCER |
780 brookside drive |
|
spencer IN 47460 |
|
Manufacturer Contact |
nancy
cutino
|
100 boston scientific way |
marlborough, MA 01752
|
5086834000
|
|
MDR Report Key | 6376016 |
MDR Text Key | 69020916 |
Report Number | 3005099803-2017-00590 |
Device Sequence Number | 1 |
Product Code |
EOQ
|
UDI-Device Identifier | 08714729861416 |
UDI-Public | (01)08714729861416(17)20181031(10)18494359 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K151315 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
02/07/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/03/2017 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Operator |
Physician
|
Device Expiration Date | 10/31/2018 |
Device Model Number | M00558250 |
Device Catalogue Number | 5825 |
Device Lot Number | 18494359 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 02/07/2017 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 10/21/2015 |
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 |