BIOVANCE INDICATIONS FOR USE

BIOVANCE is an allograft intended for use as a biological membrane covering that provides the extracellular matrix. As a barrier membrane, BIOVANCE is intended to protect the underlying tissue and preserve tissue plane boundaries. Indications include, but are not limited to, surgical covering, wrap or barrier, application to partial- and full-thickness, acute and chronic wounds (such as, traumatic and complex wounds, burns, surgical and Mohs surgery sites; and diabetic, venous, arterial, pressure and other ulcers), including wounds with exposed tendon, muscle, bone or other vital structures.

CONTRAINDICATIONS, WARNINGS, AND PRECAUTIONS

BIOVANCE is contraindicated in patients with a known hyper-sensitivity to BIOVANCE. If a patient has an adverse reaction related to the use of BIOVANCE, immediately discontinue its use. BIOVANCE should not be used on clinically infected wounds.

The pouch contents are sterile if the pouch is unopened and undamaged. Do not use if package seal is broken. Discard material if mishandling has caused possible damage or contamination. Do not resterilize.

BIOVANCE must be used prior to the expiration date on the product pouch. BIOVANCE should not be used together with a collagenase product on the wound.

For product information, product complaints, or adverse reaction reporting, call 1-844-963-2273. Please refer to the BIOVANCE Package Insert for complete product information.

BIOVANCE•3L INDICATIONS FOR USE

BIOVANCE 3L Ocular is an allograft intended for use as a biological membrane covering that provides an extracellular matrix. As a barrier membrane, BIOVANCE 3L Ocular is intended to protect the underlying tissue and preserve tissue plane boundaries. Applications include, but are not limited to, corneal and conjunctival related injuries or defects such as corneal epithelial defects, pterygium repair, fornix reconstruction, and other procedures.

CONTRAINDICATIONS, WARNINGS, AND PRECAUTIONS

BIOVANCE•3L Ocular is contraindicated in patients with a known hyper-sensitivity to BIOVANCE•3L Ocular.

If a patient has an adverse reaction related to the use of BIOVANCE•3L Ocular, immediately discontinue its use. BIOVANCE•3L Ocular should not be used on clinically infected wounds.

The pouch contents are sterile if the pouch is unopened and undamaged. Do not use if package seal is broken. Discard material if mishandling has caused possible damage or contamination. Do not resterilize.

BIOVANCE•3L Ocular must be used prior to the expiration date on the product pouch. BIOVANCE•3L Ocular should not be used together with a collagenase product on the wound. For product information or adverse reaction reporting, telephone 1-844-963-2273.
Please refer to the BIOVANCE•3L Package Insert for complete product information.