Brand Name | MAGNESIUM |
Type of Device | PHOTOMETRIC METHOD, MAGNESIUM |
Manufacturer (Section D) |
A.I.D.D LONGFORD |
lisnamuck |
co. longford |
longford N39E9 32 |
EI N39E932 |
|
Manufacturer (Section G) |
A.I.D.D LONGFORD |
lisnamuck |
co. longford |
longford N39E9 32 |
EI
N39E932
|
|
Manufacturer Contact |
siobhan
wright
|
lisnamuck |
post market surveillance |
longford N39 E-932
|
EI
N39 E932
|
433331157
|
|
MDR Report Key | 14885564 |
MDR Text Key | 297229827 |
Report Number | 3005094123-2022-00138 |
Device Sequence Number | 1 |
Product Code |
JGJ
|
UDI-Device Identifier | 00380740176532 |
UDI-Public | 00380740176532 |
Combination Product (y/n) | N |
Reporter Country Code | UK |
PMA/PMN Number | K181748 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
07/01/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 07/01/2022 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 09/18/2022 |
Device Model Number | 08P1934 |
Device Catalogue Number | 08P19-34 |
Device Lot Number | 33108UD00 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 06/08/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 11/24/2021 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Treatment | ALNTY C PROCESSING MODU, 03R67-01, AC02078 |