ARISTA AH ABSORBABLE HEMOSTAT UNKAA097

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,study report with the FDA on 2019-10-25 for ARISTA AH ABSORBABLE HEMOSTAT UNKAA097 manufactured by Davol Inc., Sub. C.r. Bard, Inc..

MAUDE Entry Details

Report Number1213643-2019-10240
MDR Report Key9238492
Report SourceHEALTH PROFESSIONAL,STUDY
Date Received2019-10-25
Date of Report2019-10-25
Date Mfgr Received2019-10-04
Date Added to Maude2019-10-25
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 ContactANNA SMITH
Manufacturer Street100 CROSSINGS BLVD.
Manufacturer CityWARWICK RI 02886
Manufacturer CountryUS
Manufacturer Postal02886
Manufacturer Phone4018258449
Manufacturer G1MEDCHEM PRODUCTS, INC. -1223089
Manufacturer Street160 NEW BOSTON STREET
Manufacturer CityWOBURN MA 01801
Manufacturer CountryUS
Manufacturer Postal Code01801
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARISTA AH ABSORBABLE HEMOSTAT
Generic NameAGENT, ABSORBABLE HEMOSTATIC, NON COLLAGEN BASED
Product CodeLMG
Date Received2019-10-25
Model NumberNA
Catalog NumberUNKAA097
Lot NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDAVOL INC., SUB. C.R. BARD, INC.
Manufacturer Address100 CROSSINGS BLVD. WARWICK RI 02886 US 02886


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-10-25

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