MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-10-28 for PSI-TEC III ASPIRATOR WITHOUT PNEUMATIC POWER SOURCE PTASPIII110 manufactured by Mentor Texas.
Report Number | 1645337-2019-22618 |
MDR Report Key | 9246001 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-10-28 |
Date of Report | 2019-10-07 |
Date of Event | 2019-10-07 |
Date Mfgr Received | 2019-11-05 |
Date Added to Maude | 2019-10-28 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. GABRIEL ALFAGEME |
Manufacturer Street | 3041 SKYWAY CIRCLE NORTH |
Manufacturer City | IRVING TX 75038 |
Manufacturer Country | US |
Manufacturer Postal | 75038 |
Manufacturer Phone | 949789-868 |
Manufacturer G1 | MENTOR TEXAS |
Manufacturer Street | 3041 SKYWAY CIRCLE NORTH |
Manufacturer City | IRVING TX 75038 |
Manufacturer Country | US |
Manufacturer Postal Code | 75038 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PSI-TEC III ASPIRATOR WITHOUT PNEUMATIC POWER SOURCE |
Generic Name | SYSTEM, SUCTION, LIPOPLASTY |
Product Code | MUU |
Date Received | 2019-10-28 |
Catalog Number | PTASPIII110 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MENTOR TEXAS |
Manufacturer Address | 3041 SKYWAY CIRCLE NORTH IRVING TX 75038 US 75038 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-28 |