Note: Clinical results may vary.
Product Information
Note: The results presented herein are case-specific and should not be used to draw general conclusions as to clinical outcomes
Cytal Wound Matrix
DEVICE DESCRIPTION
Cytal® Wound Matrix is composed of a porcine-derived extracellular matrix also known as urinary bladder matrix. The devices are supplied in a fenestrated sheet configuration and packaged in double peel-open pouches. The devices are terminally sterilized using electron beam irradiation.
INDICATIONS
Cytal Wound Matrix is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/ grafts, post-Moh’s surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one-time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. Exposure to contaminated or infected field can lead to rapid breakdown of device.
2. If active infection is present, treat patient to resolve infection prior to device application.
3. Do not use if cracked, broken, or otherwise damaged.
PRECAUTIONS
Always use aseptic technique when handling device.
MicroMatrix UBM Particulate
DEVICE DESCRIPTION
MicroMatrix® UBM Particulate is composed of a porcine-derived extracellular matrix known as urinary bladder matrix. The device is supplied in a particle form in units up to 1000mg and packaged in a glass vial and peel-open pouch. The device is terminally sterilized using electron beam irradiation.
INDICATIONS
MicroMatrix is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Moh’s surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one-time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. If active infection is present, treat patient to resolve infection prior to device application.
2. Do not use glass vial if cracked, broken, or otherwise damaged.
3. MicroMatrix is not indicated for treatment of alopecia.
PRECAUTIONS
Do not tap glass vial with metal objects or handle in a way that may cause glass to break and contaminate wound.