MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-13 for HUDSON MASK,HIGH CONC,ADULT,INTL 41007 manufactured by Teleflex Medical.
Report Number | 3004365956-2019-00212 |
MDR Report Key | 8887963 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-08-13 |
Date of Report | 2019-07-26 |
Date of Event | 2019-06-21 |
Date Mfgr Received | 2019-08-28 |
Date Added to Maude | 2019-08-13 |
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 | KATHARINE TARPLEY |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194334854 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | PARQUE INDUSTRIAL FINSA |
Manufacturer City | NUEVO LAREDO 88275 |
Manufacturer Country | MX |
Manufacturer Postal Code | 88275 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON MASK,HIGH CONC,ADULT,INTL |
Generic Name | MASK, OXYGEN |
Product Code | BYG |
Date Received | 2019-08-13 |
Returned To Mfg | 2019-08-14 |
Catalog Number | 41007 |
Lot Number | UNKNOWN |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | RESEARCH TRIANGLE PARK NC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-13 |