DERMABOND ADVANCED 0.7ML - 6EA ANX6

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-10 for DERMABOND ADVANCED 0.7ML - 6EA ANX6 manufactured by Ethicon Inc..

MAUDE Entry Details

Report Number2210968-2020-01051
MDR Report Key9687418
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-10
Date of Report2020-01-14
Date of Event2019-12-18
Date Mfgr Received2020-02-13
Device Manufacturer Date2018-09-20
Date Added to Maude2020-02-10
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 ContactKARA DITTY-BOVARD
Manufacturer StreetP.O. BOX 151, ROUTE 22 WEST
Manufacturer CitySOMERVILLE NJ 08876
Manufacturer CountryUS
Manufacturer Postal08876
Manufacturer Phone6107428552
Manufacturer G1ETHICON INC.-SAN LORENZO PR
Manufacturer StreetROAD 183, KM. 8.3
Manufacturer CitySAN LORENZO 00754
Manufacturer Postal Code00754
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDERMABOND ADVANCED 0.7ML - 6EA
Generic NameADHESIVE, TOPICAL SKIN
Product CodeMPN
Date Received2020-02-10
Returned To Mfg2020-01-29
Catalog NumberANX6
Lot NumberMKJ834
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerETHICON INC.
Manufacturer AddressP.O. BOX 151, ROUTE 22 WEST SOMERVILLE NJ 08876 US 08876


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-10

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