Eviva® EV-501 polysulfone (PSU) is offered for use in implantable medical devices. Eviva® EV-500 is the neat version of the polymer and Eviva® EV-501 is an opaque white grade.
The manufacturing facility for Eviva® PSU in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied.
Our biomaterials manufacturing processes are carefully validated and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited.
An FDA MAF is available.
The manufacturing facility for Eviva® PSU in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied.
Our biomaterials manufacturing processes are carefully validated and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited.
An FDA MAF is available.
Markets
Chemical categories
| Chemical category | Chemical family | Chemical product |
|---|
Product Functions
- Biocompatible
- Bromine Free
- Low VOC
- Good Dimensional Stability
- Alkali Resistant
- Alcohol Resistant
- Detergent Resistant
- Hydrolysis Resistant
- Low Moisture Absorption
- Non Flammable
- Flame Retardant
- Good Impact Resistant
- Low CLTE
- Radiotranslucent
- Transparency
- Radiation (Gamma) Resistant
- Laser Weldable
- Low Warpage
- Good Processing Stability
- Autoclave Sterilizable (steam)
- E-beam Sterilizable
- Radiation Sterilizable
- Ethylene Oxide Sterilizable
- Heat Sterilizable
- Good Thermal Stability
- High Heat Resistant
Format
| Physical form |
|---|
Pellets |
Region of availability
- Not available in Africa & Middle East
- Not available in Asia Pacific
- Europe
- Not available in Latin America
- Not available in North America
Eviva® EV-501 polysulfone (PSU) is offered for use in implantable medical devices. Eviva® EV-500 is the neat version of the polymer and Eviva® EV-501 is an opaque white grade. The manufacturing facility for Eviva® PSU in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterials manufacturing processes are carefully validated and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. An FDA MAF is available.