Description

Collagraft is a specialized biomaterial composite designed for bone grafting and tissue engineering applications. This product is engineered to provide an osteoconductive scaffold that supports new bone formation, combining biocompatibility with structural integrity. It is essential for medical device manufacturers, orthopedic and dental surgeons, and research institutions focused on regenerative medicine. Collagraft CAS NO 138331-02-9 represents a critical solution for bone defect repair, spinal fusion, and craniofacial reconstruction procedures.

Application

• Orthopedic Bone Grafting: Used as a bone void filler in orthopedic surgeries for trauma, spinal fusion, and joint revision.
• Dental and Maxillofacial Surgery: Serves as a scaffold for guided bone regeneration in dental implantology and craniofacial reconstruction.
• Biomedical Research: Acts as a 3D matrix for in vitro studies of cell adhesion, proliferation, and differentiation in tissue engineering.
• Medical Device Component: Incorporated into composite implants and resorbable medical devices to enhance osteointegration.
• Veterinary Orthopedics: Applied in veterinary medicine for bone repair and fusion in companion and large animals.

Basic Information

Product Name	Collagraft
CAS No.	138331-02-9
Molecular Formula	Composite Material (Contact for details)
Molecular Weight	Not Applicable
Synonyms	Collagraft Bone Graft Matrix; Collagen-Hydroxyapatite Composite; Bone Graft Substitute; Osteoconductive Biomaterial; Collagen-Calcium Phosphate Graft; Resorbable Bone Graft; Collagraft® (Registered Trade Name); Synthetic Bone Graft Material
EINECS	Contact for details

Quality Control

Our Collagraft is manufactured under strict quality systems. Each batch is tested to ensure it meets critical parameters for sterility, biocompatibility, and performance. We provide full traceability and Certificates of Analysis (COA) documenting specifications for composition, porosity, resorption rate, and mechanical strength. The production adheres to relevant medical device standards, including ISO 13485, and is suitable for applications requiring regulatory submissions.

Storage

Preserve in the original, unopened sterile packaging at a controlled room temperature (15-25°C). Protect from moisture, excessive heat, and direct light. Do not freeze or expose to gamma radiation unless specified for terminal sterilization. Once the primary packaging is opened, the product should be used immediately according to the instructions for use.

Specification

Item	Specification
Description	Sterile, off-white porous composite matrix
Composition	Collagen / Calcium Phosphate (Contact for ratio)
Porosity	> 80%
Pore Size Range	100 - 500 µm
Sterility	Sterile (Ethylene Oxide or Gamma)
Bioburden	Meets USP <71> and <85>
Pyrogens	Meets USP <151> (LAL test)
Resorption Profile	Controlled (Contact for details)
Mechanical Strength (Compressive)	Contact for details

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.