Brand Name | BA300 ABUTMENT 9MM |
Type of Device | COCHLEAR BAHA CONNECT SYSTEM |
Manufacturer (Section D) |
COCHLEAR BONE ANCHORED SOLUTIONS AB |
konstruktionsvägen 14 |
mölnlycke, 435 3 3 |
SW 435 33 |
|
Manufacturer (Section G) |
COCHLEAR BONE ANCHORED SOLUTIONS AB |
konstruktionsvägen 14 |
|
mölnlycke, 435 3 3 |
SW
435 33
|
|
Manufacturer Contact |
hemavathi
muniesparan
|
unit ug-1, vertical podium |
no. 8 jalan kerinchi, |
kuala lumpur, wilayah persekutuan 59200
|
MY
59200
|
|
MDR Report Key | 14445019 |
MDR Text Key | 292222152 |
Report Number | 6000034-2022-01533 |
Device Sequence Number | 1 |
Product Code |
LXB
|
UDI-Device Identifier | 09321502019576 |
UDI-Public | (01)09321502019576(10)COH699601(17)200424 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K100360 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
04/29/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Lay User/Patient
|
Device Expiration Date | 04/24/2020 |
Device Model Number | 92131 |
Device Catalogue Number | 92131 |
Device Lot Number | COH699601 |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
04/29/2022 |
Initial Date FDA Received | 05/19/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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 |
Patient Outcome(s) |
Required Intervention;
|
Patient Sex | Female |