BITE-GARD MOLAR BITE BLOCK 1140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2008-10-20 for BITE-GARD MOLAR BITE BLOCK 1140 manufactured by Teleflex Medical.

Event Text Entries

[980081] The event was reported as: when health care provider was changing tapes on ett tapes of the pt, the green bite-gard broke off the shank of the bite-gard. No pt injury reported. No further info available.
Patient Sequence No: 1, Text Type: D, B5


[8217003] Sample requested but not received yet. Evaluation report not available at time of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004365956-2008-00060
MDR Report Key1204672
Report Source08
Date Received2008-10-20
Date of Report2008-10-03
Date Mfgr Received2008-10-03
Date Added to Maude2009-06-11
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 FDA0
Event Location0
Manufacturer ContactANGELA BROWN, MGR, RA
Manufacturer Street4024 STIRRUP CREEK DR
Manufacturer CityDURHAM NC 27703
Manufacturer CountryUS
Manufacturer Postal27703
Manufacturer Phone9194334901
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetAVE. INDUSTRIAS NO.5954 PARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO, TAMAULIPAS 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBITE-GARD MOLAR BITE BLOCK
Generic NameBITE GARD
Product CodeJXL
Date Received2008-10-20
Catalog Number1140
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressNUEVO LAREDO, TAMAULIPAS MX


Patients

Patient NumberTreatmentOutcomeDate
10 2008-10-20

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