HUDSON BREATH CIRC,ANES,ADULT,EXP 0.5-1.8M 311403

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,user faci report with the FDA on 2019-11-01 for HUDSON BREATH CIRC,ANES,ADULT,EXP 0.5-1.8M 311403 manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number3004365956-2019-00293
MDR Report Key9268123
Report SourceDISTRIBUTOR,FOREIGN,USER FACI
Date Received2019-11-01
Date of Report2019-10-10
Date of Event2019-04-29
Date Mfgr Received2019-11-20
Device Manufacturer Date2018-06-14
Date Added to Maude2019-11-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUDSON BREATH CIRC,ANES,ADULT,EXP 0.5-1.8M
Generic NameCIRCUIT, BREATHING (W CONNECTO
Product CodeCAI
Date Received2019-11-01
Returned To Mfg2019-10-31
Catalog Number311403
Lot Number74F1801765
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-01

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.