REN? TRANSORAL NEEDLE 12-000-00-ND1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-02-28 for REN? TRANSORAL NEEDLE 12-000-00-ND1 manufactured by Cytophil, Inc..

MAUDE Entry Details

Report Number3007225376-2020-00001
MDR Report Key9772232
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-02-28
Date of Report2020-03-26
Date of Event2020-01-20
Date Mfgr Received2020-01-31
Device Manufacturer Date2019-06-04
Date Added to Maude2020-02-28
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 ContactMRS EVA HOLLFELDER
Manufacturer Street2485 CORPORATE CIRCLE SUITE 2
Manufacturer CityEAST TROY, WI
Manufacturer CountryUS
Manufacturer Phone6422765
Manufacturer G1CYTOPHIL, INC.
Manufacturer Street2485 CORPORATE CIRCLE SUITE 2
Manufacturer CityEAST TROY, WI
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameREN? TRANSORAL NEEDLE
Generic NameNEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
Product CodeGAA
Date Received2020-02-28
Model Number12-000-00-ND1
Lot NumberS912-00032
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCYTOPHIL, INC.
Manufacturer Address2485 CORPORATE CIRCLE SUITE 2 EAST TROY, WI US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-28

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