MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-11-13 for DUO FLUID CART WITH SMOKE EVACUATOR N/A 00514010200 manufactured by Dornoch.
Report Number | 0001954182-2019-00074 |
MDR Report Key | 9314932 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2019-11-13 |
Date of Report | 2019-11-13 |
Date of Event | 2019-11-08 |
Date Mfgr Received | 2019-11-08 |
Date Added to Maude | 2019-11-13 |
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 | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DRIVE |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | DORNOCH |
Manufacturer Street | 200 NORTHWEST PARKWAY |
Manufacturer City | RIVERSIDE MO 64150 |
Manufacturer Country | US |
Manufacturer Postal Code | 64150 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DUO FLUID CART WITH SMOKE EVACUATOR |
Generic Name | APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED |
Product Code | JCX |
Date Received | 2019-11-13 |
Model Number | N/A |
Catalog Number | 00514010200 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DORNOCH |
Manufacturer Address | 200 NORTHWEST PARKWAY RIVERSIDE MO 64150 US 64150 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-13 |