SINGLE FUNCTION HANDPIECE ABC PENCIL 130344

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-11-01 for SINGLE FUNCTION HANDPIECE ABC PENCIL 130344 manufactured by Consolidated Medical Equipment.

MAUDE Entry Details

Report Number3007305485-2019-00383
MDR Report Key9267265
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-11-01
Date of Report2019-11-01
Date Mfgr Received2019-10-24
Device Manufacturer Date2018-10-29
Date Added to Maude2019-11-01
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 ContactMELANIE LANNON
Manufacturer Street11311 CONCEPT BOULEVARD
Manufacturer CityLARGO FL 33773
Manufacturer CountryUS
Manufacturer Postal33773
Manufacturer Phone7273995209
Manufacturer G1CONSOLIDATED MEDICAL EQUIPMENT
Manufacturer StreetALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA
Manufacturer City31136
Manufacturer CountryMX
Manufacturer Postal Code31136
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSINGLE FUNCTION HANDPIECE ABC PENCIL
Generic NameABC PENCILS
Product CodeHAM
Date Received2019-11-01
Catalog Number130344
Lot Number201810294
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONSOLIDATED MEDICAL EQUIPMENT
Manufacturer AddressALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA 31136 MX 31136


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-01

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