BIOGLUE SURGICAL ADHESIVE BG3510-5-J

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2020-01-14 for BIOGLUE SURGICAL ADHESIVE BG3510-5-J manufactured by Cryolife, Inc. ? Kennesaw.

MAUDE Entry Details

Report Number1063481-2020-00079
MDR Report Key9586197
Report SourceDISTRIBUTOR,FOREIGN
Date Received2020-01-14
Date of Report2020-02-19
Date Facility Aware2019-12-17
Date Mfgr Received2019-12-17
Date Added to Maude2020-01-14
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 ContactROCHELLE MANEY
Manufacturer Street1655 ROBERTS BLVD
Manufacturer CityKENNESAW GA 30144
Manufacturer CountryUS
Manufacturer Postal30144
Manufacturer Phone7704193355
Manufacturer G1CRYOLIFE, INC.
Manufacturer Street1655 ROBERTS BLVD. NW
Manufacturer CityKENNESAW GA 30144
Manufacturer CountryUS
Manufacturer Postal Code30144
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOGLUE SURGICAL ADHESIVE
Generic NamePATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
Product CodeDXZ
Date Received2020-01-14
Model NumberBG3510-5-J
Lot NumberUNKNOWN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCRYOLIFE, INC. ? KENNESAW
Manufacturer Address1655 ROBERTS BLVD. NW KENNESAW GA 30144 US 30144


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-14

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