MMG LT100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2001-07-17 for MMG LT100 manufactured by Rusch, Inc..

Event Text Entries

[17481581] The customer reports that the tubes were cracked.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1045162-2001-00130
MDR Report Key342938
Report Source04
Date Received2001-07-17
Date of Report2001-07-16
Date Mfgr Received2001-07-11
Date Added to Maude2001-07-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactDONNA MCLEOD, QUALITY ADMIN.
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30096
Manufacturer CountryUS
Manufacturer Postal30096
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMMG
Generic NameDISPOSABLE ASPIRATOR TUBE
Product CodeBYZ
Date Received2001-07-17
Model NumberNA
Catalog NumberLT100
Lot Number*
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key332274
ManufacturerRUSCH, INC.
Manufacturer Address5335 DIVIDEND DR. DECATUR GA 30035 US
Baseline Brand NameMMG STERILE ASPRI-TRAP (ASPIRATING TUBE)
Baseline Model NoNA
Baseline Catalog NoLT100
Baseline IDNA
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2001-07-17

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