PE ADULT-PED DRY/ WET LF 6/CS A-6000-08LF

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-09-24 for PE ADULT-PED DRY/ WET LF 6/CS A-6000-08LF manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number3004365956-2019-00253
MDR Report Key9112010
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-09-24
Date of Report2019-09-03
Date of Event2019-08-31
Date Mfgr Received2019-09-03
Date Added to Maude2019-09-24
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
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 NamePE ADULT-PED DRY/ WET LF 6/CS
Generic NameBOTTLE, COLLECTION, VACUUM
Product CodeKDQ
Date Received2019-09-24
Catalog NumberA-6000-08LF
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-24

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