HEMOPATCH Sealing Hemostat Room Temperature (RT)

When outcomes count, reach for HEMOPATCH Sealing Hemostat.

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Why Choose HEMOPATCH Sealing Hemostat?

Reduce Post-Operative Complications

Hemopatch Sealing Hemostat may decrease post-operative pancreatic fistulas, CSF leakage, and can help avoid transfusions in cardiac surgery as compared to the standard of care. Reducing these post-operative complications may result in substantial cost savings.1-5*

*Transfusions: Hemopatch Sealing Hemostat 23.5% vs Comparator 34% (p=0.24)

Strong Adherence to the Tissue Surface

Hemopatch Sealing Hemostat rapidly adheres to applied tissue due to the electrophilic cross-linking action of NHS-PEG.6 The patch provides mechanical structure to support friable tissue.6

Designed for Utmost Flexibility

The soft, thin and flexible collagen pad allows easy handling and preparation for MIS applications. No preparation or pre-moistening is required.7

Effective Hemostasis

92% of surgeons rated Hemopatch Sealing Hemostat as highly satisfactory for its ease of use, handling, flexibility/pliability and tissue adherence characteristics in open and laparoscopic procedures.8 Successful hemostasis after two minutes of approximation occurred in 93% of patients.8

The Benefits of Room Temperature

Storage in the Operating Room

Hemopatch Sealing Hemostat RT can be stored directly in the O.R. suture cabinet at room temperature (2°C–30°C) eliminating the need for refrigeration.7

Rapid Tissue Adherence

Enhanced PEG stability also improves tissue adherence and reliable hemostatic and sealing performance.7,9

Enhanced Product Stability

The new packaging enhances product stability, making it more convenient and reliable without changing its core functionality.9

Extended Shelf Life

Hemopatch Sealing Hemostat RT has a longer shelf life and can be stored for up to 36 months.9

Why the Change?

Hemopatch in the Operating Room

Addressing Customer Needs

The transition to a room temperature patch reflects our commitment to addressing the needs of our Healthcare Professionals and the staff that support them.

Handing over a Hemopatch

When Ease of Use Counts, Reach for HEMOPATCH Sealing Hemostat

Hemopatch Sealing Hemostat RT can eliminate the need for cold-chain storage, allowing for room temperature storage (2°C–30°C) for up to 36 months.7,9

It is now easily stored in the operating room, reducing the need for advance preparation or trips to a refrigerator during critical surgical procedures.

Cutting a Hemopatch

Sustainability and Efficiency

Smaller, optimized packaging7,9 reduces storage space requirements and contributes to lower waste generation.

These improvements may offer cost savings for hospitals and align with broader goals for environmental sustainability.

Hemopatch in Hand

Comprehensive Surgical Confidence

Hemopatch Sealing Hemostat RT is a safe, effective solution that delivers fast hemostasis in mild to moderate bleeding, robust tissue sealing, and seamless integration with host tissue.7

Offers improved surgical outcomes and cost savings by helping avoid transfusions and enhancing patients' recovery and care.1-5,10

Hemopatch Packaging Comparison

Optimized Packaging

Hemopatch Sealing Hemostat RT has a smaller, optimized packaging size,reducing storage space requirements and contributing to lower waste generation.

Hemopatch Ordering Codes

Ordering Information

Hemopatch Sealing Hemostat RT has new product codes for ordering.9 Download the technical sheet to save or share with your staff. 

Frequently Asked Questions

HEMOPATCH Sealing Hemostat Indications and Important Safety Information

INDICATIONS:

Hemopatch Sealing Hemostat is indicated as a hemostatic device and surgical sealant across various soft tissues (cardiovascular, connective tissue, parenchyma, serosa, viscera), and dura for procedures in which control of mild or moderate bleeding or leakage of other body fluids or air by conventional surgical techniques is either ineffective or impractical. Hemopatch Sealing Hemostat may be used to augment dura closure techniques to close small dural defects (≤3mm) following traumatic injury, excision, retraction or shrinkage of the dura mater.

INTENDED PURPOSE:

Hemopatch Sealing Hemostat is an absorbable collagen pad intended for sealing and hemostasis.

CONTRAINDICATIONS:

Do not compress Hemopatch Sealing Hemostat into blood vessels or use intravascularly. The device must not be used in patients with known hypersensitivity to bovine proteins or brilliant blue (FD&C Blue No. 1 (Blue 1)).

WARNINGS:

Hemopatch Sealing Hemostat is not intended to be used in pulsatile, severe bleeding. The use of Hemopatch Sealing Hemostat is not recommended in the presence of an active infection. When used in, around, or in proximity to foramina in bone, areas of bony confine, the spinal cord, the brain and/or cranial nerves, care should be exercised to avoid overpacking (collagens may expand upon absorption of liquid), creating the potential for neural damage. Hemopatch Sealing Hemostat is not intended as a substitute for meticulous surgical technique and the proper application of ligatures or other conventional procedures for hemostasis and sealing.

For safe and proper use of Hemopatch Sealing Hemostat, refer to full Instructions for Use.