MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-09-30 for TRUCLEAR 7210165 manufactured by Smith & Nephew.
Report Number | 1643264-2019-20020 |
MDR Report Key | 9135984 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2019-09-30 |
Date of Report | 2019-09-30 |
Date of Event | 2019-09-01 |
Date Mfgr Received | 2019-09-05 |
Date Added to Maude | 2019-09-30 |
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 |
Reporter Occupation | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | LISA HERNANDEZ |
Manufacturer Street | 5920 LONGBOW DRIVE |
Manufacturer City | BOULDER CT 80301 |
Manufacturer Country | US |
Manufacturer Postal | 80301 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | SMITH & NEPHEW |
Manufacturer Street | 150 MINUTEMAN RD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRUCLEAR |
Generic Name | INSUFFLATOR, HYSTEROSCOPIC |
Product Code | HIG |
Date Received | 2019-09-30 |
Returned To Mfg | 2019-09-19 |
Model Number | 7210165 |
Catalog Number | 7210165 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW |
Manufacturer Address | 150 MINUTEMAN RD ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-30 |