HemoPore®
bioresorbable
nasal dressing

5400-020-208

8 cm, 8-pack

With chitosan lactate blended directly into our proprietary synthetic polymer HemoPore bioresorbable nasal dressing delivers reliable tissue support and hemostatic control. HemoPore dressing provides a great option for nurses and emergency room providers to treat epistaxis.

Instruction for use IFU LIBRARY Product catalog VIEW PDF

HemoPore ER Placement Videos

Watch the below videos for a comprehensive view of how to place HemoPore in an Emergency care setting to treat epistaxis. If you have any other questions, please reach out to your local Stryker ENT representative.

HemoPore in-service training video

The in-service video features Dr. Chhabra demonstrating how to place HemoPore with the instruments available in an Emergency care setting.

HemoPore placement endoscope footage

The video of the HemoPore placement features two angles, the HemoPore being inserted externally and the intranasal footage of where it is being placed inside the nasal cavity.

Dr. Chhabra is a paid consultant of Stryker. His/her statements represent his/her own opinions based on personal experience and are not necessarily those of Stryker. Individual results may vary.

HemoPore fragmentable nasal dressing Indications for Use: HemoPore is intended for use in patients undergoing nasal/sinus surgery as a temporary wound dressing. HemoPore functions as a topical hemostatic aid to control mild bleeding by tamponade effect, blood absorption, platelet activation and aggregation. It acts as an adjunct to aid in the natural healing process as a space occupying stent to separate and support tissues. It prevents adhesions and minimizes edema.

The dressing is a biodegradable, polyurethane foam that fragments within several days. The nasal dressing drains from the nasal cavity via natural mucus flow and/or irrigation. HemoPore is indicated for use as a nasal packing to treat epistaxis.

HemoPore fragmentable nasal dressing contraindications: HemoPore should not be used on patients who have known allergies to shellfish.

Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.

Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.

This document is intended solely for the use of healthcare professionals. A surgeon must always rely on his or her own professional clinical judgment when

deciding whether to use a particular product when treating a particular patient. We do not dispense medical advice and recommend that surgeons be trained in the use of any particular product before using it in surgery.

The information presented is intended to demonstrate Stryker’s products. A surgeon must always refer to the package insert, product label and/or instructions for use, including the instructions for cleaning and sterilization (if applicable), before using any of Stryker’s products. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your representative if you have questions about the availability of Stryker’s products in your area.

Stryker or its affiliated entities own, use, or have applied for the following trademarks or service marks: HemoPore and Stryker. All other trademarks are trademarks of their respective owners or holders.

The absence of a product, feature, or service name, or logo from this list does not constitute a waiver of Stryker’s trademark or other intellectual property rights concerning that name or logo.