Brand Name | ABDOMINAL BINDER |
Type of Device | BINDER, ABDOMINAL |
Manufacturer (Section D) |
ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A. |
km 20.5 carretera a villa |
canales zona 3 finca morancito |
villa canales, 01065, guatemala |
GT |
|
Manufacturer (Section G) |
ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A. |
km 20.5 carretera a villa |
canales zona 3 finca morancito |
villa canales, 01065, guatemala |
GT
|
|
Manufacturer Contact |
melissa
logsdon
|
200 debusk lane |
powell, TN 37849
|
8653626157
|
|
MDR Report Key | 18310541 |
MDR Text Key | 330281226 |
Report Number | 3010452421-2023-00009 |
Device Sequence Number | 1 |
Product Code |
FSD
|
UDI-Device Identifier | 00749756283281 |
UDI-Public | 00749756283281 |
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
12/12/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/12/2023 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Model Number | 13662067 |
Device Lot Number | 55074867 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 11/27/2023 |
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 11/15/2023 |
Was Device Evaluated by Manufacturer? |
Yes
|
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 |
|
|