Syringe - VanishPoint

Transcription

0086
Syringe
Standard Draw Procedure
1
In-Patient, Automated Retraction
Non-Reusable
2
4
3
Product Usage Information:
1. Prepare and give injection using aseptic technique according to institutional policy.
2. For injection into patients, continue depressing plunger to activate automatic needle retraction while needle is
still in patient. For injection into IV ports, continue depressing plunger to activate automatic needle retraction
and immediately remove needle from port. Full dose is administered only when needle retraction is activated.
3. Needle will automatically retract into syringe, preventing exposure to contaminated needle and rendering
syringe non-reusable. In the event that needle retraction mechanism does not activate, discard syringe in an
appropriate sharps container per protocol of institution. Do not recap contaminated needles.
4. Dispose of VanishPoint® syringe in an appropriate sharps container per protocol of institution.
Precautions:
• Single use only. Reuse of this device may result in exposure to bloodborne pathogens, including Hepatitis B
virus (HBV), Hepatitis C virus (HCV), and human immunodeficiency virus (HIV).
• Contents are sterile, non-toxic, and non-pyrogenic. Do not use if product or package is damaged.
• Not made with natural rubber latex.
• Use only with attached needle. Needle cannot be changed.
• Automated needle retraction occurs only when barrel is emptied and plunger is fully depressed.
• For applications where full dose is not administered, expel remaining contents according to institutional
policy and activate needle retraction.
• U.S. Federal Law restricts this device to sale by or on the order of a physician.
511 Lobo Lane
Little Elm, Texas 75068-0009
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M001 Rev. 9 EN, JUL 2013
© 2003, 2013 Retractable Technologies, Inc. All rights reserved.
0086
Suggested Technique For TB Skin Testing Using
1mL VanishPoint ® Tuberculin Syringe
2. Using other hand, fully depress plunger to activate automatic needle retraction while needle
is still in patient. Full dose is administered only when needle retraction is activated.
3. Needle will automatically retract into syringe, preventing exposure to contaminated needle and
rendering syringe non-reusable. In the event that needle retraction mechanism does not activate,
discard syringe in an appropriate sharps container per protocol of institution. Do not recap
contaminated needles.
511 Lobo Lane
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M032 REV.1 EN, AUG 2013
0086
U-100 Insulin Syringe
Standard Draw Procedure
In-Patient, Automatic Retraction
Non-Reusable
2. For injection into patients, continue depressing plunger to activate automatic needle retraction
while needle is still in patient. Full dose is administered only when needle retraction is activated.
3. Needle will automatically retract into syringe, preventing exposure to contaminated needle and
rendering syringe non-reusable. In the event that needle retraction mechanism does not activate,
discard syringe in an appropriate sharps container per protocol of institution. Do not recap
Precautions:
• Use U-100 Insulin only.
• Single use only. Reuse of this device may result in exposure to bloodborne pathogens, including
Hepatitis B virus (HBV), Hepatitis C virus (HCV), and human immunodeficiency virus (HIV).
• Contents are sterile, non-toxic, and non-pyrogenic. Do not use if product or package is damaged.
• Not made with natural rubber latex.
• Use only with attached needle. Needle cannot be changed.
• Automated needle retraction occurs only when barrel is emptied and plunger is fully depressed.
• U.S. Federal Law restricts this device to sale by or on the order of a physician.
511 Lobo Lane
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M036 REV.1 EN, Aug 2013
Blood Collection Tube Holder
1
2
3
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VanishPoint
Van
ishP
oin
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®
®
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Vanis
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®
1. Securely thread multiple sample blood collection needle into tube holder. Remove needle cover when ready to use
2. Perform venipuncture per protocol of institution.
3. Insert blood collection tube into tube holder, pushing forward to start blood flow. Remove blood collection tube
when filled and repeat with additional tubes as required. For small diameter tubes, use VanishPoint® small diameter
tube adapter with tube holder.
4. Once last tube has been removed and needle is still in patient’s vein, close end cap securely into tube holder.
5. Needle will automatically retract from patient’s vein into tube holder. In the event that needle retraction mechanism
does not activate, discard tube holder in an appropriate sharps container per protocol of institution. Do not recap
6. Dispose of tube holder in an appropriate sharps container per protocol of institution.
Precautions:
•
•
•
•
•
•
•
Single use only. Reuse of this device may result in exposure to bloodborne pathogens, including Hepatitis B virus
(HBV), Hepatitis C virus (HCV), and human immunodeficiency virus (HIV).
Do not use if product is damaged.
Not made with natural rubber latex.
For use with conventional multiple sample blood collection needles up to 1 1/2” (38 mm) in length.
Not for use with winged needle sets or luer adapters.
Do not attempt to remove blood collection needle from tube holder after retraction.
U.S. Federal Law restricts this device to sale by or on the order of a physician.
511 Lobo Lane
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M002 REV.3 EN, AUG 2013
0086
Blood Collection Set
•
Select and prepare venipuncture site using aseptic technique according to
institutional policy.
•
For blood collection using a tube holder, thread the luer adapter into a tube
holder, while ensuring winged hub remains tightly connected to adapter.
•
For blood collection using a syringe, remove luer adapter and attach syringe.
Dispose of luer adapter in an appropriate sharps container per protocol of
institution.
•
Holding device using the finger grips, carefully remove needle cover.
1. Perform venipuncture, observing for blood return in device. Collect blood
specimen according to institutional policy.
1
2
2. Once blood collection is complete and the needle is still in the patient’s vein,
depress retraction trigger indicated by the color-coded arrow (◄ ).
3. The needle will automatically retract from the patient’s vein into the device.
In the event that needle retraction mechanism does not activate, discard blood
collection set in an appropriate sharps container per protocol of institution.
Do not recap contaminated needles.
4. Dispose of blood collection set and tube holder (or syringe) in an appropriate
sharps container per protocol of institution. Do not remove tube holder from
blood collection set. For blood collection using a syringe, transfer blood to
appropriate specimen container per institutional protocol.
3
Precautions:
•
Single use only. Reuse of this device may result in exposure to bloodborne
pathogens, including Hepatitis B virus (HBV), Hepatitis C virus (HCV), and
human immunodeficiency virus (HIV).
•
Do not use if product or package is damaged.
•
•
Not made with DEHP.
•
Not made with PVC.
•
The VanishPoint® blood collection set can be used for blood collection for
diagnostic purposes or for short term IV administration, up to 2 hours. The
same set should not be used for both procedures.
•
U.S. Federal Law restricts this device to sale by or on the order of a physician.
4
511 Lobo Lane
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M035 REV.3 EN, MAR 2014
0086
I.V. Catheter
•
•
1.
2.
3.
4.
•
•
•
Select and prepare site using aseptic technique according to institutional policy.
Based on patient allergy information, select an antiseptic solution to disinfect the
insertion site. Recommended solutions include: 2% chlorhexidine, 10% providoneiodine, 70% alcohol.
Remove needle cover and inspect catheter unit.
Perform venipuncture, observing for blood return. Advance the catheter slightly
to assure full catheter entry into the vein.
Holding the flashback chamber stationary, disengage the hub from the introducer
needle and advance the catheter into the vein. DO NOT REINSERT THE
NEEDLE INTO THE CATHETER AT ANY TIME.
Before withdrawing the introducer needle from the catheter, depress the color
coded end of the needle housing to activate1the automated retraction of the
introducer needle. To activate the retraction mechanism using one hand, stabilize
the color coded end of the needle housing against the proximal portion of the palm,
while pulling back the housing using the finger grips.
The introducer needle will retract into the housing. In the event that needle
retraction mechanism does not activate, discard catheter introducer in an
appropriate sharps container per protocol of institution. Do not recap contaminated
needles.
Dispose of the introducer needle in an appropriate sharps container per protocol
of institution.
Securely connect tubing or adapter to the catheter
hub, following the
3
manufacturer’s instruction for the device. 1
Secure catheter and dress site per protocol of institution.
1
2
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24
34
2
4
Precautions:
•
•
•
•
•
•
•
•
•
Single use only. Reuse of this device may result in exposure to bloodborne
pathogens, including Hepatitis B virus (HBV), Hepatitis C virus (HCV), and
human immunodeficiency virus (HIV).
Do not use if product or package is damaged.
To prevent exposure to contaminated needle,
3 activate safety mechanism prior
to withdrawing needle from catheter.
Do not use scissors or sharp implements near I.V. catheters.
Never reinsert the introducer needle into the catheter.
Clinicians must follow instructions for use and be trained on proper product use.
During catheter insertion, maintenance, replacement, and removal, follow current
“Guidelines for the Prevention of Intravascular Catheter-Related Infections,”
Centers for Disease Control and Prevention, Atlanta, GA.
Notify physician immediately and follow facility protocols in the event patients
exhibit symptoms of infusion-related complications.
4
View from underside of palm
511 Lobo Lane
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M003 REV.3 EN, AUG 2013

Syringe - VanishPoint

Transcription

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