NEOCONNECT GRAVITYPRO PNM-S100NCV

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-11 for NEOCONNECT GRAVITYPRO PNM-S100NCV manufactured by Neomed, Inc..

MAUDE Entry Details

Report Number3006520777-2019-00007
MDR Report Key8995174
Date Received2019-09-11
Date of Report2019-09-10
Date of Event2019-07-22
Report Date2019-07-29
Date Reported to FDA2019-07-29
Date Reported to Mfgr2019-08-06
Date Mfgr Received2019-08-12
Device Manufacturer Date2017-08-03
Date Added to Maude2019-09-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. MELINDA SMITH
Manufacturer Street100 LONDONDERRY COURT SUITE 112
Manufacturer CityWOODSTOCK GA 30188
Manufacturer CountryUS
Manufacturer Postal30188
Manufacturer Phone7705162225
Manufacturer G1SYNECCO, CO., LTD.
Manufacturer StreetB801 RONGAN PLAZA, NO. 700 SOUTH TIANTONG ROAD
Manufacturer CityNINGBO, 315100
Manufacturer CountryCH
Manufacturer Postal Code315100
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEOCONNECT GRAVITYPRO
Generic NameENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS
Product CodePNR
Date Received2019-09-11
Returned To Mfg2019-09-03
Model NumberPNM-S100NCV
Catalog NumberPNM-S100NCV
Lot Number20170720
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNEOMED, INC.
Manufacturer Address100 LONDONDERRY COURT SUITE 112 WOODSTOCK GA 30188 US 30188


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-11

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