| About |
|---|
| Versaflex™ G2705 N is an easy processing material designed for applications where FDA regulations are required. The material exhibits high resilience, low compression set, and good puncture resealing characteristics. It is also steam sterilizable. Versaflex™ G2705 N supplied as a dense pellet.&& |
| Product Description | |
|---|---|
| Supplier | Polyone |
| Generic | TPE |
| Material Status | Commercial: Active |
| Availabilitys | Africa & Middle East ,North America,Latin America,Asia Pacific,Europe |
| Process Methods | Injection Molding |
| Technical Data | |||
|---|---|---|---|
| MECHANICAL | Nominal value | Unit | Test method |
| Shore hardness | |||
| Shore A, 10 seconds, 23 ℃ | 60 | ASTM D2240 | |
| elastic body | Nominal value | Unit | Test method |
|---|---|---|---|
| tensile strength | |||
| fracture | 4.62 | MPa | ASTM D412 |
| 300% strain | 3.64 | MPa | ASTM D412 |
| Tensile strain | |||
| fracture | 470 | % | ASTM D412 |
| tear strength | 22.6 | kN/m | ASTM D624 |
| Compression deformation | |||
| 23℃ | 20 | % | ASTM D395B |
| PHYSICAL | Nominal value | Unit | Test method |
|---|---|---|---|
| Density | 0.888 | g/cm³ | ASTM D792 |
| Apparent viscosity of melt | |||
| 200℃，11200 sec^-1 | 14.9 | Pa·s | ASTM D3835 |
| Process Conditions | |||
|---|---|---|---|
| injection | Nominal value | Unit | Test method |
| Squeeze description | Nominal value | Unit | Test method |
| Extrusion | Nominal value | Unit | Test method |
| Barrel rear temperature | 171 to 199 | °C | |
| Barrel middle temperature | 182 to 216 | °C | |
| Barrel front temperature | 182 to 216 | °C | |
| Nozzle temperature | 193 to 227 | °C | |
| Mold temperature | 27 to 49 | °C | |
| Back pressure | 0.689 to 1.38 | MPa | |
| Screw speed | 25 to 100 | rpm | |
| Melt temperature | 191 to 238 | °C | |
| Nozzle temperature | 191 to 238 | °C | |
| Notes |
|---|
| 1. Please contact PolyOne GLS Thermoplastic Elastomers for a complete copy of the GLS Healthcare Policy. 1. The Customer must notify GLS of any FDA Class I and/or European Union Class I medical devices for each specific product and application. 2. The Customer shall not knowingly manufacture, use, sell or otherwise supply, directly or indirectly products or compounds made from GLS products in any of the following without prior written approval by GLS for each specific product or application: a. Cosmetics b. Drugs and other Pharmaceuticals c. Temporary or permanent implantation in the human body, regardless of the intended duration of implantation d. Class II and Class III Medical Devices as defined in 21 CFR 860.3 (“Medical Devices”) e. Class IIa, IIb and III as defined in Directive 93/42/EEC |
| 2. Typical properties: these are not to be construed as specifications. |
| 3. Die C |
| 4. 2 hr |
| 【 Disclaimer 】 Guangzhou Soliao Information Technology Co., Ltd. reserves all rights. The information in this data table was obtained from the manufacturer of the material on soliao.com. Soliao.com makes every effort to ensure the accuracy of this data. However, the search company does not assume any responsibility for the uncertainty and consequences caused to users by these data values and suggestions, and strongly recommends verifying the data values with the material supplier before the final selection of materials. |