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Interfyl®

Interfyl® Human Connective Tissue Matrix is an allogeneic decellularized particulate human placental connective tissue matrix.

Celularity, Inc.

Celularity Inc. is a biotechnology company that produces cells and tissues derived from the postpartum placenta. Its portfolio of products supports the body's ability to regenerate tissue and includes BIOVANCE® Human Amniotic Membrane Allograft and Interfyl® Human Connective Tissue Matrix
Toll free:(844) 963-2273 Website: www.celularity.com
Benefits

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

Indications

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).

Contraindications

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

Warnings and Precautions

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 Effects/Reactions

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.

Storage Requirements

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

How Supplied/Sizing
Particulate: 50mg, 100mg. Flowable: 0.3ml, 0.6ml, 1ml, 1.5ml, 100mg.
HCPCS Code
Product features
check_circle Assigned HCPCS code
cancel Minimally manipulated
cancel Cryopreserved
check_circle Dehydrated
check_circle Desiccated
check_circle Flowable
check_circle Micronized
cancel Sheet form
cancel Requires refrigeration
check_circle Shelf life greater than 2 years
cancel Shelf life limited
check_circle Indicated for acute wounds
check_circle Indicated for chronic wounds
check_circle Indicated for diabetic ulcers
check_circle Indicated for pressure ulcers
check_circle Indicated for surgical wounds
cancel Indicated for third-degree burns
check_circle Indicated for venous ulcers
cancel Contact manufacturer for usage guidelines
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
check_circle Published Clinical Article Available
Recommended Use

Acute Wounds
Burns
Cavity Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Palliative Wounds
Pressure Ulcers
Surgical Wounds
Superficial Wounds
Traumatic Wounds
Venous Ulcers

Mode of Use/Application

Aseptic technique. Apply topically. Product may be used "dry" for placement to desired area or mixed with saline or other sterile fluid for wet application. Based on physician preference and/or clinical application, the consistency can be altered by adding more or less liquid.

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