en
4. Use an appropriate sized trocar to allow mesh to slide down the trocar with
minimal force.
5. If fixation is used, B
ard
®
permanent or absorbable fixation devices or non-
absorbable monofilament sutures are recommended to properly secure the
device. If other fixation devices are used, they must be indicated for use in
hernia repair.
6. If fixation is used, care should be taken to ensure that the mesh is
adequately fixated to the abdominal wall. If necessary, additional fasteners
and/or sutures should be used.
ADVERSE REACTIONS:
Possible complications include seromas, adhesions, hematomas, inflamma-
tion, extrusion, fistula formation and recurrence of the hernia or soft tissue
defect.
TRACEABILITY:
A traceability label which identifies the type, size, expiration date, and lot num-
ber of the device is attached to every package. This label should be affixed to
the patient’s permanent medical record to clearly identify the device that was
implanted.
only
Bard, 3DMax, and Davol are trademarks and/or registered trademarks of
C. R. Bard, Inc., or an affiliate.
Copyright © 2009, 2011 C. R. Bard, Inc. All Rights Reserved.
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Contents
Do not use if package is damaged
Nonabsorbable
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