NeoPly® Amniotic Membrane
NeoPly® is an amniotic membrane that is sterile and ready to use.
• Ready to use
• Stored at room temperature
NeoPly® should not be implanted into: (1) areas with active or latent infection; and/or (2) into a patient with a disorder that would create an unacceptable risk of post-operative complications.
Do not re-sterilize.
Store at ambient temperature. Keep away from excessive heat. Do not freeze.
NeoPly® is intended for single patient use. Do not reuse.
Do not use if: package integrity has been violated, opened or damaged; mishandling has caused possible damage or contamination; seal is broken or compromised.
Once NeoPly® has expired, it must be discarded.
Do not implant in the presence of active infection.
After use, handle and dispose of all unused portions and packaging in accordance with accepted medical practice and applicable local, state and federal laws and regulations.
NeoPly® may contain trace amounts of antibiotic residuals such as gentamicin used in low doses and rinsed during processing.
As with any surgical procedure, the possibility of infection exists.
Dedicated processing and sterilization methods are employed to eliminate deleterious properties of the allograft. However, as with all biological implants, the possibility of rejection exists.
Any adverse reactions, including the suspected transmission of disease attributable to this allograft, should be immediately reported to Lucina BioSciences, LLC.
Store at 15°C-30°C.
|Assigned HCPCS code|
|Shelf life greater than 2 years|
|Shelf life limited|
|Indicated for acute wounds|
|Indicated for chronic wounds|
|Indicated for diabetic ulcers|
|Indicated for pressure ulcers|
|Indicated for surgical wounds|
|Indicated for third-degree burns|
|Indicated for venous ulcers|
|Contact manufacturer for usage guidelines||●|
Lucina BioSciences, LLC is a research and development, manufacturing and distribution corporation that produces cutting edge, placental derived products using their proprietary Nativus process.