MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-17 for INTEGRITY TEMPORARY CROWN & BRIDGE MATERIAL-CARTRIDGE SYSTEM 666220 manufactured by Dentsply Caulk.
Report Number | 2515379-2019-00028 |
MDR Report Key | 9204596 |
Date Received | 2019-10-17 |
Date of Report | 2019-10-11 |
Date of Event | 2019-09-05 |
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 | DENTSPLY CAULK |
Manufacturer Street | 38 W. CLARK AVE. |
Manufacturer City | MILFORD DE 19963 |
Manufacturer Country | US |
Manufacturer Postal Code | 19963 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | INTEGRITY TEMPORARY CROWN & BRIDGE MATERIAL-CARTRIDGE SYSTEM |
Generic Name | CROWN AND BRIDGE, TEMPORARY, RESIN |
Product Code | EBG |
Date Received | 2019-10-17 |
Returned To Mfg | 2019-10-02 |
Model Number | NA |
Catalog Number | 666220 |
Lot Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DENTSPLY CAULK |
Manufacturer Address | 38 W. CLARK AVE. MILFORD DE 19963 US 19963 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-10-17 |