NEOTECH PRODUCTS UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-02-12 for NEOTECH PRODUCTS UNKNOWN manufactured by Neotech Products Llc.

MAUDE Entry Details

Report Number2025917-2020-00001
MDR Report Key9702394
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-02-12
Date of Report2020-02-12
Date of Event2019-12-31
Date Mfgr Received2020-01-14
Date Added to Maude2020-02-12
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 ContactBEN MAHAJAN
Manufacturer Street28430 WITHERSPOON PARKWAY
Manufacturer CityVALENCIA, CA
Manufacturer CountryUS
Manufacturer Phone7757466147
Manufacturer G1NEOTECH PRODUCTS LLC
Manufacturer Street28430 WITHERSPOON PARKWAY
Manufacturer CityVALENCIA, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEOTECH PRODUCTS
Generic NameNEOBAR
Product CodeCBH
Date Received2020-02-12
Model NumberUNKNOWN
Catalog NumberUNKNOWN
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNEOTECH PRODUCTS LLC
Manufacturer Address28430 WITHERSPOON PARKWAY VALENCIA, CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-12

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