Brand Name | BURR, 4.5MM, 15DEG, BALL BURR, 5/PK |
Type of Device | BURR |
Manufacturer (Section D) |
GYRUS ACMI INC. |
136 turnpike road |
southborough MA 01772 210 |
|
Manufacturer (Section G) |
GYRUS ACMI INC. |
136 turnpike road |
|
southborough MA 01772 210 |
|
Manufacturer Contact |
noemi
schambach
|
2400 ringwood ave. |
san jose, CA 95131
|
4089355002
|
|
MDR Report Key | 3807239 |
MDR Text Key | 4388935 |
Report Number | 2951238-2014-00121 |
Device Sequence Number | 1 |
Product Code |
HBE
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
User Facility |
Reporter Occupation |
Not Applicable
|
Type of Report
| Initial |
Report Date |
02/28/2014 |
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 | BUR45151BB |
Device Catalogue Number | BUR45151BB |
Device Lot Number | IH806301 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
02/28/2014
|
Initial Date FDA Received | 03/20/2014 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 11/22/2013 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
Yes
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
|
|