BLAKEMORE TUBE 204803180

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2003-01-24 for BLAKEMORE TUBE 204803180 manufactured by Willy Rusch Ag.

Event Text Entries

[18446253] Hole in large balloon.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610520-2003-00014
MDR Report Key439875
Report Source06
Date Received2003-01-24
Date of Report2003-01-24
Date Mfgr Received2003-01-09
Date Added to Maude2003-01-30
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 Location0
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 NameBLAKEMORE TUBE
Generic NameESOPHAGEAL
Product CodeKDH
Date Received2003-01-24
Model NumberNA
Catalog Number204803180
Lot Number229222
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key428811
ManufacturerWILLY RUSCH AG
Manufacturer AddressWILLY-RUSCH STRASSE 4-10 KERNEN I.R. GM 71394
Baseline Brand NameBLAKEMORE TUBE
Baseline Model NoNA
Baseline Catalog No204803180
Baseline IDNA
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]60
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2003-01-24

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