Medical Device Index: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z


CATHETER, ELECTROPHYSIOLOGY ALLIANCE MEDICAL CORPORATION Reports 1998-2010
Medical Device Brand Name: DAIG
Medical Device Generic Name: CATHETER, ELECTROPHYSIOLOGY
Medical Device Manufacturer Name:ALLIANCE MEDICAL CORPORATION


CATHETER, ELECTROPHYSIOLOGY ALLIANCE MEDICAL CORPORATION Report # 714359
MD OPENED A REPROCESSED DAIG 5F CRD-2 CATHETER; AFTER PLACING THE DISTAL TIP IN THE SHEATH, MD WENT TO CONNECT IT TO THE CONNECTOR AND IT LOOKED FUNNY. LOOKING BACK AT THE STERILE TABLE, THE HUB WAS STILL ON THE DRAPE. IT APPEARS THE ADHESIVE IN THE OUTER HUB CAME APART FROM THE INNER SHAFT HUB.

CATHETER, ELECTROPHYSIOLOGY ALLIANCE MEDICAL CORPORATION Report # 691547
SUPRA CS CATHETER IN USE TO ACCESS THE CS, CORONARY SINUS, VEIN. THIS DEVICE WAS ON ITS SECOND REPROCESSING BY ALLIANCE, AND WAS FOUND TO HAVE AN INCORRECT CURVE AT THE DISTAL END AND HAD TO BE REMOVED FROM THE PATIENT AND REPLACED WITH ANOTHER CATHETER.


Loading

Please Share Your CATHETER, ELECTROPHYSIOLOGY ALLIANCE MEDICAL CORPORATION Experience, Join the Discussion:
Source: Manufacturer and User Facility Device Experience Database - (MAUDE). MAUDE data represents reports of adverse events involving medical devices. The data consists of voluntary reports since June 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August 1996. MAUDE may not include reports made according to exemptions, variances, or alternative reporting requirements granted under 21 CFR 803.19. MAUDE is scheduled to be updated quarterly and the search page reflects the date of the most recent update. MAUDE data is not intended to be used either to evaluate rates of adverse events or to compare adverse event occurrence rates across devices. Please be aware that reports regarding device trade names may have been submitted under different manufacturer names. Searches only retrieve records that contain the search term(s) provided by the requester. The data is updated on a quarterly basis. DISCLAIMER: Section 21 CFR 803.16 states that "A report or other information submitted by a reporting entity under this part, and any release by FDA of that report or information, does not necessarily reflect a conclusion by the party submitting the report or by FDA that the report or information constitutes an admission that the device, or the reporting entity or its employees, caused or contributed to the reportable event. The reporting entity need not admit and may deny that the report or information submitted under this part constitutes an admission that the device, the party submitting the report, or employees thereof, caused or contributed to a reportable event." In addition, some firms have submitted their own additional disclaimer statements. A file of those disclaimers will be placed on the web shortly.
PatientsVille.com does not provide medical advice, diagnosis or treatment. The information contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments.The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider.We hope you found our information about b>CATHETER, ELECTROPHYSIOLOGY ALLIANCE MEDICAL CORPORATION.