Amniotic tissue is recovered f rom healthy mothers who have undergone full-term delivery
Rampart is processed in accordance with FDA regulations and AATB standards
The amniotic membrane has distinct non-immunological attributes
Requires no up-f ront preparation
Ambient temperature storage
Can be applied on either side of the sheet
E-Beam sterilization provides a sterility assurance level (SAL) of 10-6
PRODUCT DETAILS
Rampart’s protective amnion properties create an ideal barrier to protect soft tissue from the surrounding environment. Processed with minimal manipulation, it retains the qualities of the native extracellular matrix (ECM). Rampart can be applied in any orientation, quickly hydrates in situ, and naturally stays in place, eliminating application placement limitations.
The product is a barrier to protect:
Diabetic ulcers
Venous ulcers
Pressure ulcers
Burns
Wounds with exposed tendons, muscles, or bones
Proteins in the product include:
Collagen I, III, IV, V, and VII
Elastina
Fibronectin
Laminin
OUR PŪRAMP PROCESS
Tissue collection
Placental tissue is donated
from live births in the U.S.
without harming the mother
or baby
Donor screening
A thorough medical and social
history is obtained for each
donor to ensure eligibility
requirements are met
Infectious disease testing
• HBsAg
•HBcAb
• HCVAb
• HCV NAT
• HBV NAT
• HIV NAT
• HIV 1/2Ab
• WNV NAT
• HTLV I/II
Ab
• RPR/STS
Tissue processing
All tissue undergoes a
proprietary cleansing process
to remove blood contaminants
and reduce bioburden
Tissue sterilization
Tissue is sterilized for an
additional level of safety,
achieving a sterility
assurance level (SAL) of 10-6