Brand Name | BIA210 FLANGE FIXTURE ST 4MM W ABUTMENT 5.5MM |
Type of Device | COCHLEAR BAHA CONNECT SYSTEM |
Manufacturer (Section D) |
COCHLEAR BONE ANCHORED SOLUTIONS AB |
konstruktionsvägen 14 |
po box 82 |
mölnlycke, 435 2 2 |
SW 435 22 |
|
Manufacturer (Section G) |
COCHLEAR BONE ANCHORED SOLUTIONS AB |
konstruktionsvägen 14 |
po box 82 |
mölnlycke 43533 |
SW
43533
|
|
Manufacturer Contact |
bianca
pries
|
1 university avenue |
macquarie university, nsw 2109
|
AS
2109
|
|
MDR Report Key | 6970153 |
MDR Text Key | 90024448 |
Report Number | 6000034-2017-01906 |
Device Sequence Number | 1 |
Product Code |
LXB
|
UDI-Device Identifier | 09321502018982 |
UDI-Public | (01)09321502018982(10)COH139328(17)140901 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K984162 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
user facility |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
10/02/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 10/23/2017 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Lay User/Patient
|
Device Expiration Date | 09/01/2014 |
Device Model Number | 92135 |
Device Catalogue Number | 92135 |
Device Lot Number | COH139328 |
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 10/02/2017 |
Date Device Manufactured | 09/17/2009 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
Patient Age | 18 YR |