MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-06-24 for NOMAD DENTAL 60KV 0.850.0000 FP 0001 manufactured by Aribex.
Report Number | 1017522-2019-00011 |
MDR Report Key | 8726362 |
Report Source | DISTRIBUTOR,HEALTH PROFESSION |
Date Received | 2019-06-24 |
Date of Report | 2019-06-21 |
Date of Event | 2019-04-09 |
Date Mfgr Received | 2019-04-09 |
Device Manufacturer Date | 2012-02-09 |
Date Added to Maude | 2019-06-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
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. DAVID WATERS |
Manufacturer Street | 11727 FRUEHAUF DRIVE |
Manufacturer City | CHARLOTTE NC 28273 |
Manufacturer Country | US |
Manufacturer Postal | 28273 |
Manufacturer Phone | 7045877297 |
Manufacturer G1 | ARIBEX |
Manufacturer Street | 11727 FRUEHAUF DRIVE |
Manufacturer City | CHARLOTTE NC 28273 |
Manufacturer Country | US |
Manufacturer Postal Code | 28273 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NOMAD DENTAL 60KV |
Generic Name | EXTRAORAL SOURCE X-RAY SYSTEM |
Product Code | EHD |
Date Received | 2019-06-24 |
Returned To Mfg | 2019-04-12 |
Model Number | 0.850.0000 |
Catalog Number | FP 0001 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ARIBEX |
Manufacturer Address | 11727 FRUEHAUF DRIVE CHARLOTTE NC 28273 US 28273 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-24 |