SENOMARK ULTRA MARKER SMMA11R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-16 for SENOMARK ULTRA MARKER SMMA11R manufactured by Bard Peripheral Vascular, Inc..

MAUDE Entry Details

Report Number2020394-2019-04042
MDR Report Key9200135
Date Received2019-10-16
Date of Report2019-10-16
Date Mfgr Received2019-09-30
Date Added to Maude2019-10-16
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 ContactJUDITH LUDWIG
Manufacturer Street1415 W. 3RD STREET
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1INFUS MEDICAL (THAILAND)
Manufacturer Street706 MOO 4 BANGPOO IND ESTATE
Manufacturer CitySAMUTPRAKARN PROVINCE 10280
Manufacturer CountryTH
Manufacturer Postal Code10280
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSENOMARK ULTRA MARKER
Generic NameBREAST TISSUE MARKER
Product CodeNEU
Date Received2019-10-16
Model NumberSMMA11R
Catalog NumberSMMA11R
Lot NumberVTCP00083
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-16

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