POOLE INSTRUMENT W/3.05 MTR TUBING 20/CS 0035070

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 2019-08-30 for POOLE INSTRUMENT W/3.05 MTR TUBING 20/CS 0035070 manufactured by Consolidated Medical Equipment.

MAUDE Entry Details

Report Number3007305485-2019-00303
MDR Report Key8949474
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-08-30
Date of Report2019-10-15
Date Mfgr Received2019-09-04
Device Manufacturer Date2018-09-04
Date Added to Maude2019-08-30
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 ContactMS TRACEY WEISELBENTON
Manufacturer Street11311 CONCEPT BLVD
Manufacturer CityLARGO FL 337734908
Manufacturer CountryUS
Manufacturer Postal337734908
Manufacturer Phone7273995557
Manufacturer G1CONSOLIDATED MEDICAL EQUIPMENT
Manufacturer StreetALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA
Manufacturer CityCHIHUAHUA, 31136
Manufacturer CountryMX
Manufacturer Postal Code31136
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOOLE INSTRUMENT W/3.05 MTR TUBING 20/CS
Generic NameAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED
Product CodeGCX
Date Received2019-08-30
Returned To Mfg2019-09-04
Catalog Number0035070
Lot Number201809045
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCONSOLIDATED MEDICAL EQUIPMENT
Manufacturer AddressALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA CHIHUAHUA, 31136 MX 31136


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-30

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