MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-05-09 for AH PLUS JET 606.20.118 manufactured by Dentsply Detrey Gmbh.
Report Number | 8010638-2019-00006 |
MDR Report Key | 8596252 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-05-09 |
Date of Report | 2019-05-08 |
Date Mfgr Received | 2019-04-08 |
Date Added to Maude | 2019-05-09 |
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 DETREY GMBH |
Manufacturer Street | DETREY STRASSE 1 |
Manufacturer City | KONSTANZ, 78467 |
Manufacturer Country | GM |
Manufacturer Postal Code | 78467 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AH PLUS JET |
Generic Name | RESIN, ROOT CANAL FILLING |
Product Code | KIF |
Date Received | 2019-05-09 |
Returned To Mfg | 2019-04-30 |
Model Number | NA |
Catalog Number | 606.20.118 |
Lot Number | 1806000796 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DENTSPLY DETREY GMBH |
Manufacturer Address | DETREY STRASSE 1 KONSTANZ, 78467 GM 78467 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-05-09 |