EndoShield 2
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At End of Life (continued)
End of Life Indicators
Discontinue use if any of the following are evident:
Intermittent electrical performance.
The device indicates a low or dead battery condition. See the
Troubleshooting and
System Maintenance
section for indications of low or dead battery.
Reprocessing
WARNING:
This product shall not be reprocessed.
Compatible Products
For successful operation, the EndoShield 2 must be used with the following compatible
products.
Caution:
Use of other accessories or cables may result in increased EMC emissions or
decreased immunity.
Electrosurgical Generator
Electrosurgical Generator (ESU)
Encision Adapter Required
Manufacturer
Model
Conmed
System 5000
ES9007
Covidien
Force Triad
N/A
Force FX
N/A
Force FX-C
N/A
FT10
N/A
Erbe
VIO 300 D
N/A
Megadyne
MegaPower
N/A
WARNING:
The electrosurgical generators referenced here have been tested for use
with the EndoShield 2. Use of an untested ESU may result in an inoperative active
electrode monitoring system.
Caution:
All electrosurgical generators must have a contact quality monitoring circuit
for return electrodes.
Return Electrode
The EndoShield 2 requires a dual-area patient return electrode.
Active Electrode
The foot-control instrument must have patented AEM technology and be
manufactured by/for Encision Inc., or licensed by Encision Inc.
Hand-control AEM instruments are not compatible with the EndoShield 2.
Instrument Cord
The cord connecting the foot-controlled instrument to the EndoShield 2 must have
patented AEM technology and be manufactured by/for Encision Inc., or licensed by
Encision Inc.
Encision Adapter
Some electrosurgical generators require an adapter for setup of the EndoShield 2
(see the Electrosurgical Generator table above). Refer to the
System
Setup
section for
proper connections.
