TIDI 2100NOCH Nasal Oxygen Cannula Hydrocolloid Securement Device Instructions
- June 1, 2024
- TIDI
Table of Contents
TIDI 2100NOCH Nasal Oxygen Cannula Hydrocolloid Securement Device
For lines and tubes sized 4.5 – 19 Fr.
Specifications
| REF | 2100NOCH |
|---|---|
| Brand | Grip-Lok® |
| Hypoallergenic | Yes |
| Manufacturer | TIDI® Products, LLC |
| Address | 570 Enterprise Drive, Neenah, WI 54956 USA |
| Phone | +1 920 751 4300 |
| Website | tidiproducts.com/securement |
| Expiration Date | 2024-03-12 |
Instructions
Intended for use in the general population, for adhesive securement of the catheter hub, tube or line to the patient’s skin.
- Select the area for the placement of the Grip-Lok. Note: The tube should be already positioned on the patient.
- Prepare the skin according to the standard hospital protocol for dressing application. Skin must be clean and dry. Hair removal may be required on some patients for better adhesion.
- Remove the bottom liner by holding fabric section and pulling off liner (Fig 1). Do not remove the top liner at this time. The top liner should now be removed.
- Place the Grip-Lok on the site by continuing to hold by the fabric and press onto the skin with gentle pressure.
- Position the tube in the center of the top exposed adhesive strip between the fabric and the white hook section.
- Secure the tube by folding over the fabric section until it meets with the white hook portion and apply gentle pressure to the back of the entire fabric area (Fig 2).
- Note: The Grip-Lok may be slightly warmed between hands prior to application for optimal adhesion.
- Note: To remove or adjust secured tube, hold hydrocolloid adhesive down to skin while opening top fabric section.
- Note: The Grip-Lok 2100NOCH may be cut in half prior to removal of liners to reduce the size.
- Direction: For additional skin protection, use skin prep pad prior to application of stabilization device.
- Note: Use of an alcohol swab or saline solution may be used to aid in removal.
- If you experience severe redness, itching, swelling, or irritation of the skin, consult your physician as this may be a sign of an allergic reaction.
- Re-use of this device may change its mechanical or biological features and may cause device failure, allergic reactions or bacterial infections.
- Replace securement device if soiled or saturated in fluid or if device shows signs of wear or damage.
- Note: If being used in a medical facility, dispose according to medical facility and municipal guidelines. Do not use if the product’s sterile barrier system or its packaging is compromised.
Product Images
- Fig. 1: Image showing the bottom liner being removed by holding the fabric section.
- Fig. 2: Image displaying the Grip-Lok securing a tube on a patient’s face with the top liner removed and the adhesive section exposed.
FAQ
What sizes of lines and tubes can be secured with the Grip-Lok 2100NOCH? It is designed for lines and tubes sized 4.5 – 19 Fr. Is the Grip-Lok hypoallergenic? Yes, this product is hypoallergenic. Can the Grip-Lok be reused? Re-use of this device is not recommended as it may alter its features and increase the risk of failure, allergic reactions, or infections. How should the Grip-Lok be disposed of? In a medical facility, dispose of it according to medical facility and municipal guidelines. Can the Grip-Lok be warmed before use? Yes, it may be slightly warmed between hands prior to application for better adhesion. How do you use the Grip-Lok? Follow the provided step-by-step instructions for placement and securement of the tube.
TIDI® Support Caregivers. Protect Patients.
Grip-Lok is a registered trademark of TIDI Products, LLC.
May be patented: see www.tidiproducts.com/virtual-patent- marking
TIDI® Products, LLC
570 Enterprise Drive
Neenah, WI 54956 USA
Phone: +1920751 4300
tidiproducts.com/securement
Grip-Lok is a registered trademark of TIDI Products, LLC.
May be patented: see www.tidiproducts.com/virtual-patent-
marking