MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-10-17 for E3 6:1 CONTRA ANGLE E3CONTRA manufactured by Tulsa Dental Products Llc.
Report Number | 2320721-2019-00215 |
MDR Report Key | 9205090 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-10-17 |
Date of Report | 2019-10-16 |
Date Mfgr Received | 2019-09-16 |
Date Added to Maude | 2019-10-17 |
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 | DENTIST |
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 | ADVANCED TECHNOLOGY RESEARCH (A.T.R.) S.R.L. |
Manufacturer Street | VIA SAN DONATO 1 |
Manufacturer City | PISTOIA, 51100 |
Manufacturer Country | IT |
Manufacturer Postal Code | 51100 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | E3 6:1 CONTRA ANGLE |
Generic Name | CONTROLLER, FOOT, HANDPIECE AND CORD |
Product Code | EBW |
Date Received | 2019-10-17 |
Model Number | NA |
Catalog Number | E3CONTRA |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TULSA DENTAL PRODUCTS LLC |
Manufacturer Address | 608 ROLLING HILLS DRIVE JOHNSON CITY TN 37604 US 37604 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-17 |