VACUETTE? TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 454322

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-02-21 for VACUETTE? TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 454322 manufactured by Greiner Bio-one Gmbh.

MAUDE Entry Details

Report Number8020040-2016-00019
MDR Report Key9741944
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-02-21
Date of Report2020-02-21
Date Mfgr Received2015-11-22
Device Manufacturer Date2015-07-24
Date Added to Maude2020-02-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMANFRED ABEL
Manufacturer Street4238 CAPITAL DRIVE
Manufacturer CityMONROE NC 28110
Manufacturer CountryUS
Manufacturer Postal28110
Manufacturer Phone7042617800
Manufacturer G1GREINER BIO-ONE NA INC
Manufacturer Street4238 CAPITAL DRIVE
Manufacturer CityMONROE NC 28110
Manufacturer CountryUS
Manufacturer Postal Code28110
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVACUETTE? TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2%
Generic NameTUBES, VACUUM SAMPLE, WITH ANTICOAGULANT
Product CodeGIM
Date Received2020-02-21
Model Number454322
Catalog Number454322
Lot NumberA15073SN
Device Expiration Date2017-01-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerGREINER BIO-ONE GMBH
Manufacturer AddressBAD HALLER STR. 32 KREMSMUNSTER, AUSTRIA 4550 AU 4550


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-21

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