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Idiomas disponibles
Catheter Stabilization Device
Read carefully before use.
Safety and Efficacy Considerations:
Rx only. Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
Sterilized by Ethylene Oxide.
Single use only.
Do not resterilize.
Do not use if package is damaged. Fluid path (if present) is nonpyrogenic.
Product code,
lot number and expiration date information – see packaging.
S
L
ock ®
Do not alter the
or components. Procedure must be performed by trained personnel with
tat
knowledge of anatomical landmarks, safe technique and potential complications.
LATEX FREE
Indications for use:
® stabilization device is for compatible medical tubes and catheters.
The S
L
tat
ock
Contraindications:
Known tape or adhesive allergies.
Warnings and Precautions:
® stabilization device where loss of adherence could occur, such as with
1. Do not use the S
L
tat
ock
a confused patient, diaphoretic or nonadherent skin or when the access device is not monitored
daily .
2. Observe universal blood and body fluid precautions and infection control procedures, during
® stabilization device.
application and removal of the S
L
tat
ock
® STABILIZATION DEVICE PAD TO SKIN IF DESIRED OR DEEMED
3. SUTURE THE S
L
tat
ock
NECESSARY.
® stabilization device contact with alcohol or acetone, both can weaken bonding
4. Avoid the S
L
tat
ock
® stabilization device pad adherence.
of components and the S
L
tat
ock
5. Minimize catheter/tube manipulation during application and removal of the S
device.
6. Remove oil and moisturizer from targeted skin area.
® stabilization device pad adherence and catheter/tube position should be routinely
7. The S
L
tat
ock
inspected.
® stabilization device so arrow points toward catheter tip.
8. Orient the S
L
tat
ock
® stabilization device should be replaced at least every 7 days.
9. The S
L
tat
ock
10. This is a single use device. Reuse and/or repackaging may create a risk of patient or user
infection, compromise the structural integrity and/or essential material and design characteristics
of the device, which may lead to device failure, and/or lead to injury, illness or death of the
patient.
11. Do not re-sterilize. The sterility of the single use device is not guaranteed following re-sterilization
because of an indeterminable degree of potential pyrogenic or microbial contamination which
may lead to infectious complications. Re-sterilization may compromise the structural integrity,
essential material and/or design characteristics and may lead to an unpredictable loss of
functionality and/or device failure.
® stab lization device. See illustrations for specific
Use sterile technique for app ication and removal of the S
L
tat
ock
details.
Application:
® stabilization device area as follows:
1. PREP: Prepare the targeted S
L
tat
ock
a. Alcohol - to degrease skin and remove Betadine, then
b. Skin prep (if included) - to enhance adherence and protect skin, then
ALLOW TO DRY COMPLETELY.
ENGLISH
2. PRESS: Before applying the S
tat
® stabilization device retainer.
the S
L
tat
ock
® stabilization device paper backing, and
3. PEEL: Peel off the S
L
tat
ock
® stabilization device on targeted skin one side at a time
4. PLACE: Place the S
L
tat
ock
Note:
® stabilization device pad can be adhered after X-ray confirmation of proper catheter/
•
The S
L
tat
ock
tube position.
Removal:
Carefully remove overlying dressing using stretch technique and sutures (if applicable).
® stabilization device adhesive with alcohol swab while gently lifting the
1. DISSOLVE the S
L
tat
ock
® stabilization device pad.
S
L
tat
ock
2. DISENGAGE catheter/tube from the S
® stabilization device dressing change in the patient chart.
3. DOCUMENT the S
L
tat
ock
4. DISPOSE of all equipment in appropriate containers.
Extens on Set
Indications for Use:
For use as an extension to the IV fluid delivery system. The S
set male Luer adapter is specifically designed to secure the extension set when used as part of the
® stabilization device stabilization system.
S
L
tat
ock
DELIVERY LINE
Options:
A
® stabilization
L
tat
ock
B
D
Options:
I
or
E
C
G
A
CATHETER HUB
Options / Precautions:
Needleless Valve (E) and Y-Site w/ Needleless Valve (F)
1. Connect fluid line or device to center of valve using Luer Lock connections only.
2. Do not use with a blunt tip cannula or conventional needle. If a needle must be used, attach a
PRN adapter and use as a standard injection site.
® stabilization device pad to skin, secure tube or catheter to
L
ock
® stabilization device retainer.
L
tat
ock
® stabilization device extension
L
tat
ock
Directions for Use:
Use aseptic technique.
1. Tighten all connections.
A
2. Remove Protector Caps (A)
as required.
H
3. Connect Female Port (B) to fluid
or
delivery line or device and prime/
flush.
4. Connect Male Port (C) to catheter
hub.
5. Open Slide Clamp (D) for
unimpeded flow.
6. Swab septum of injection site and
F
needleless valve (if present) with
preferred antiseptic.
General Precautions:
1. Avoid air trapped in set. Puncturing
tube can cause air embolism or
leakage.
2. Avoid contact with alcohol, it
can alter the structure of plastic
components.
T-Connector (G)
Stopcock (H)
1. Position handle over port you wish to close.
2. Open port for fluid delivery.
3. Close and cap available port when not in use.
Standard Y-S te (I)
1. Use with a conventional needle only. Do not use with a blunt tip cannula.
NOTES
1. Tubing is non-DEHP PVC
2. Dispose used set in appropriate container.
3. Replace extension set and ports per CDC guidelines.
Fill Volumes:
Micro
12" (304.8mm) ext set
4" (101.6mm) ext set with SmartSite®
6" (152.4mm) ext set with bonded MicroClave®
6" (152.4mm) ext set with SmartSite®
6" (152.4mm) ext set with UltraSite®
8" (203.2mm) ext set with 3-way stopcock
9" (228.6mm) bifurcated ext set with SmartSite® (2)
Macro
6" (152.4mm) ext set with Bonded MicroClave®
6" (152.4mm) ext set with Smart Y® and SmartSite®
6" (152.4mm) ext set with SmartSite®
6" (152.4mm) ext set with UltraSite®
Bard and StatLock are trademarks and/or registered trademarks of C. R. Bard, Inc.
All other trademarks are the property of their respective owners.
Manufacturer:
Authorized Representative in the
Bard Access Systems, Inc.
European Community
605 North 5600 West
Bard Limited
Salt Lake City, UT 84116 USA
Forest House, Brighton Road
800-443-5505, 801-522-5000
Crawley, West Sussex
www.bardaccess.com
RH11 9BP UK
Assembled in Mexico
Fill Volume (mL)
No Valve
W/Valve
0.40
NA
0.18
0.27
NA
0.26
0.25
0.34
0.25
0.62
0.36
0.55
0.57
0.75
NA
0.97
0.90
1.06
0.90
0.99
0.90
1.26
0086
2403097 1405R
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