SURGICAL TUBING 0037860

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 2019-08-28 for SURGICAL TUBING 0037860 manufactured by Consolidated Medical Equipment.

MAUDE Entry Details

Report Number3007305485-2019-00315
MDR Report Key8940145
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-08-28
Date of Report2019-10-15
Date Mfgr Received2019-10-09
Device Manufacturer Date2018-09-18
Date Added to Maude2019-08-28
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 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 NameSURGICAL TUBING
Generic NameSURGICAL TUBING
Product CodeBYY
Date Received2019-08-28
Returned To Mfg2019-09-04
Catalog Number0037860
Lot Number201809184
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 31136 MX 31136


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-28

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