Indications For Use; Contraindications - Covidien Sonicision SCDA13 Mode D'emploi

Sonicision™

SCDA13

SCDA26

SCDA39

SCDA48
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①
Clamping jaw – Holds tissue against
active blade
②
Active curved blade – Delivers energy
effect
③
Shaft
④
Shaft-rotation wheel (black)– Rotates
shaft 360°
⑤
Speaker – Emits system status tones
⑥
Dual-mode energy button (blue)-
Selects energy activation in minimum
or maximum mode
⑦
Jaw lever (black) – Closes and opens
clamping jaw
⑧
Shaft measurement marks - measures
up to 10 cm from the distal end (not
available on all models)
⑨
Battery door (black) – Closes and seals
battery compartment
⑩
Battery door release button (black) –
Opens the battery door
Do not use if package is opened or
damaged
Defibrillation-proof type BF applied
part
Curved Jaw Cordless
Ultrasonic Dissector
5 mm - 13 cm
Curved Jaw Cordless
Ultrasonic Dissector
5 mm - 26 cm
Curved Jaw Cordless
Ultrasonic Dissector
5 mm - 39 cm
Curved Jaw Cordless
Ultrasonic Dissector
5 mm - 48 cm
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Not made with natural rubber latex

Indications for Use

The Sonicision Curved Jaw Cordless Ultrasonic
Dissection Device is indicated for soft tissue
incisions when bleeding control and minimal
thermal injury are desired. The device can be
used as an adjunct to or substitute for
electrosurgery, lasers, and steel scalpels in
general, plastic, pediatric, gynecologic,
urologic, exposure to orthopedic structures
(such as spine and joint space) and other open
and endoscopic procedures. The Sonicision
Curved Jaw Cordless Ultrasonic Dissection
Device can be used to coagulate isolated
vessels up to and including 5 mm in diameter.
The Sonicision 13 cm device is also indicated
for use in otorhinolaryngologic (ENT)
procedures.

Contraindications

• The device is not indicated for incising bone.
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• The device is not intended for contraceptive
tubal occlusion.
Warning
Safe use of the Sonicision Curved Jaw
Cordless Ultrasonic Dissector requires the
user to read, understand, and follow the
accompanying instructions.
The dissector cannot be adequately cleaned
or sterilized for safe reuse and is, therefore,
intended for single use. Attempts to clean
and sterilize the dissector for reuse may result
in infection or product-failure risks to the
patient and operator.
Visually inspect all system components for
breaks, cracks, nicks, or other damage. Do not
use damaged components. Use of damaged
components may result in injury to the
patient or operator.
Contact between the active blade and other
metal objects (hemostats, clips, staples,
retractors, etc.) may result in product
damage, such as a broken blade. Pieces of a
broken blade may fall into the surgical cavity
causing unintended tissue damage.
en
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