MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-26 for X-SMART ENDO MOTOR WITH CONTRA ANGLE HANDPIECE A100400000000 manufactured by Dentsply Maillefer.
Report Number | 8031010-2019-00195 |
MDR Report Key | 9127023 |
Date Received | 2019-09-26 |
Date of Report | 2019-09-26 |
Date Mfgr Received | 2019-08-27 |
Date Added to Maude | 2019-09-26 |
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. KARL NITTINGER |
Manufacturer Street | 221 W. PHILADELPHIA ST. SUITE 60W |
Manufacturer City | YORK PA 17401 |
Manufacturer Country | US |
Manufacturer Postal | 17401 |
Manufacturer Phone | 7178494424 |
Manufacturer G1 | NAKANISHI INC. |
Manufacturer Street | 700 SHIMOHINATA |
Manufacturer City | KANUMA-SHI, 322-8666 |
Manufacturer Country | JA |
Manufacturer Postal Code | 322-8666 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | X-SMART ENDO MOTOR WITH CONTRA ANGLE HANDPIECE |
Generic Name | HANDPIECE, DIRECT DRIVE, AC-POWERED |
Product Code | EKX |
Date Received | 2019-09-26 |
Model Number | NA |
Catalog Number | A100400000000 |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DENTSPLY MAILLEFER |
Manufacturer Address | CHEMIN DU VERGER 3 BALLAIGUES, 1338 SZ 1338 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-26 |