Product Manual

© 2003, 2019 Retractable Technologies, Inc. All rights reserved.
511 Lobo Lane
Little Elm, Texas 75068-5295
Tel: (972) 294-1770 Fax: (972) 294-4400
Toll Free 1-888-703-1010
M001 REV. 11 EN, JUL 2019
Syringe
21 4
3
Standard Draw Procedure In-Patient, Automated Retraction Non-Reusable
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
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.
2797

Summary of content (1 pages)