Contraindications; Device Description - Hologic TriMark Instructions D'utilisation

Système de marquage de site de biopsie
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  • FRANÇAIS, page 10
TriMark
for Eviva
®
®
Biopsy Site Marker System
Instructions for Use
Please read all information carefully. Failure to properly follow the instructions may lead to unanticipated
surgical consequences.
Important: This package insert is designed to provide Instructions for Use of the TriMark® biopsy site
marker system for the Eviva® bopsy device system. It is not a reference to surgical techniques.
Indications
The TriMark for Eviva biopsy site marker system is indicated for use to mark an open or percutaneous
biopsy site to radiographically mark the location of the biopsy site.

Contraindications

None known.

Device Description

The TriMark for Eviva biopsy site marker system is supplied as a sterile, single patient use system,
comprised of a singular implant-grade titanium marker. The deployment device is a hand held device that
delivers the marker from the distal tip. The deployment device consists of a cannula, handle, rigid push
rod and plunger.
Deployment Device
Plunger
Hub Latch

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