Klinidur 122326 Long Stretch Compression Instruction Manual
- June 16, 2024
- Klinidur
Table of Contents
Klinidur 122326 Long Stretch Compression
Product Information
Specifications
- Product Name: Klinidur Cohesive Bandage
- Color: Beige
- Material: 100% cotton
- Coating: Latex-free cohesive coating on both sides
- Latex Content: Not made with natural rubber latex
- Medical Device: Yes
Product Description
Klinidur Cohesive bandage is an elastic, beige-colored, cohesive short stretch
compression bandage. It is made of 100% cotton with a latex-free cohesive
coating on both sides. The bandage is not made with natural rubber latex and
is classified as a medical device.
Indications
Klinidur Cohesive bandage is indicated for the treatment of venous leg ulcers
from the lower extremity, lymphatic edemas, and other clinical conditions
where compression is appropriate.
Contra-indications
There are no specific contra-indications mentioned in the user manual.
However, it is always recommended to consult with a healthcare professional
before using any medical device.
Precautions
It is important to follow the instructions for use and precautions mentioned
in the user manual. If any serious incident occurs in relation to the device,
it should be reported to Farmaban S.A., the local distributor, and the
competent healthcare authority.
Storage
The product should be stored in its original packaging in cool, dry, and well-
ventilated conditions, away from direct sunlight.
Removal and Disposal
Klinidur Cohesive bandage can be removed by either using bandage scissors or
unwrapping it. The disposal of the compression system should be done according
to the current national legislation, standards, and guidelines for the
disposal of medical waste.
Product Usage Instructions
Step 1: Preparing for Application
Before applying the Klinidur Cohesive bandage, ensure that the affected area
is clean and dry.
Step 2: Applying the Bandage
- Ensure that the desired angle is maintained throughout the entire application.
- Start by applying the bandage to the metatarsophalangeal joint (the joint at the base of the toes).
- Continue circularly wrapping the bandage, overlapping each layer by 50% to achieve proper compression.
- Continue wrapping until the desired coverage is achieved, making sure to maintain tension on the bandage.
- Secure the end of the bandage with tape or clips to prevent it from unraveling.
Step 3: Removal
To remove the Klinidur Cohesive bandage, either use bandage scissors to cut it
or simply unwrap it from the affected area.
Frequently Asked Questions (FAQ)
-
Q: Can I reuse the Klinidur Cohesive bandage?
A: No, the bandage is designed for single use only and should be disposed of after use. -
Q: How long can I wear the Klinidur Cohesive bandage?
A: The duration of wear depends on your specific condition and the recommendation of your healthcare professional. It is important to follow their instructions for the appropriate wear time. -
Q: Can I apply the bandage by myself, or do I need assistance?
A: While it is possible to apply the bandage by yourself, it may be easier and more effective to have someone assist you, especially for hard-to-reach areas. -
Q: Can I shower or swim while wearing the Klinidur Cohesive bandage?
A: It is generally recommended to avoid exposing the bandage to water while wearing it. However, you should consult with your healthcare professional for specific instructions regarding showering or swimming with the bandage on.
Product Description
- Klinidur Cohesive bandage is an elastic, beige colored, cohesive short stretch compression bandage.
- Made of 100% cotton with a latex-free cohesive coating on both sides.
Not made with natural rubber latex. Medical device.
Indications
Klinidur Cohesive bandage is indicated for the treatment of venous leg ulcers from the lower extremity, lymphatic oedemas and other clinical conditions where compression is appropriate.
Contra-indications
- Do not apply directly on open wounds or breached skin.
- Decompensated heart insufficiency
- Septic phlebitis
- Advanced diabetic microangiopathy
- Phlegmasia cerulea dolens
- Severe arterial occlusive disease in patients with an ankle-brachial pressure index (ABPI) of less than 0.8
- Known hypersensitivity to any of the materials of the components.
Directions for use
Application
- Apply the bandage with the foot in dorsiflexion (90º). Ensure that this angle is maintained throughout the entire application.
- Start by applying the bandage to the metatarsophalangeal joint in a circular manner, wrapping two turns to ¬fix the bandage. Use moderate tension and slightly elevate the lateral edge of the foot.
- Wrap the bandage over the back of the foot and secure the heel by using a figure of eight turns with minimum stretch. Ensure full coverage of the heel.
- Continue wrapping the bandage in a circular manner up the leg with a minimum stretch and an overlap of 50%. Finish bandaging around 2 cm below the popliteal space. Cut off the excess bandage, and if necessary secure with adhesive tape. Carefully press down the bandage to ensure full cohesion.
Removal and disposal
- Klinidur Cohesive bandage can be removed with bandage scissors or by unwrapping.
- Follow your current national legislation, standards, and guidelines, which regulate the disposal of medical waste for the disposal of the compression system.
Precautions
- For single use only.
- Do not reuse. Reuse can compromise product integrity or lead to device failure.
- Always apply under the supervision of a healthcare professional. It is recommended to have adequate training for the correct application of the bandage.
- Check that the patient’s ABPI is higher than 0,8 before applying the bandage.
- Patients with known arterial insufficiency, decompensated heart insufficiency, or advanced diabetic microangiopathy may not tolerate compression; it should only be used under medical prescription, with careful monitoring and after appropriate treatment.
- Wrapping too tightly may impair circulation. Monitor the area of application frequently for signs of discoloration, pain, numbness, tingling, or other changes in sensation and swelling. If these symptoms appear, patients should remove the bandage immediately and inform the healthcare professional.
- Before applying, it is necessary to perform the usual diagnostic examinations. Wounds must be cleansed and covered with wound dressings appropriate to the wound conditions.
- Follow current international guidelines and local regulations for infection control.
- If the bandage becomes wet, or loose-fitting, or when it no longer conforms to the shape of the bandaged area, it should be replaced.
Storage
- The products should be stored under ambient conditions (5°C-30°C), in the original packaging. In a cool, dry, and well-ventilated place, away from direct sunlight.
- In case a serious incident has occurred in relation to the device: Inform Farmaban S.A. as listed on the packaging, your local distributor, and your competent healthcare authority.
Manufactured by
Farmaban S.A.
- Carrer Vilella de Claret, 6 08272 Sant Fruitós de Bages Barcelona, Spain
- www.farmaban-sa.com.
Distributed by
Medeco B.V.
- Brandpuntlaan Zuid 14 2665 NZ Bleiswijk The Netherlands