Interfyl®

• Available as a particulate or flowable
• 10 year shelf life
• Ambient room temperature storage

For surgical indications:
Interfyl® is intended for use as the replacement or supplementation of damaged or inadequate integumental tissue. Indications include, but are not limited to, treatment of soft tissue voids, correction of soft tissue defects, soft tissue augmentation during repair of dehisced or complicated surgical closures and repair of small surgical defects resulting from either medical or surgical conditions including those with exposed vital structures (bone, tendon, ligament, or nerve).

For wound indications:
Interfyl® is intended for use as the replacement or supplementation of damaged or inadequate integumental tissue. Indications include, but are not limited to: augmentation of deficient/inadequate soft tissue and treatment of deep dermal wounds; surgical wounds; soft tissue voids as a result of tunneling wounds, fistula tracts, or dermal undermining-including those with exposed vital structures (bone, tendon, ligament, or nerve).

If a recipient had an adverse reaction related to previous use of Interfyl, do not re-apply.

Interfyl® should not be used in clinically infected sites. Do not use Interfyl® for intravenous, intra-arterial, intra-ocular or intrathecal applications. The contents are sterile if the vial/syringe (container) is unopened and undamaged. Do not resterilize. Interfyl® must be used prior to the expiration date on the product pouch. Once opened, Interfyl® must be used within two hours or discarded per institutional procedures.

Adverse reactions or outcomes that potentially involve the use of Interfyl® must be reported promptly to the Celularity Inc. Customer Service at 1-844-963-2273.

Store Interfyl® in its original packaging in a clean, dry environment at an ambient room temperature.