| About |
|---|
| Versaflex™ OM 3060-1 is a clear, medical compliant overmold designed to adhere to multiple substrates. Excellent bond to PC, ABS, PC/ABS, PC/PETG, and PC/PBT Rubber Feel Soft Touch&& |
| Product Description | |
|---|---|
| Supplier | Polyone |
| Generic | TPE |
| Material Status | Commercial: Active |
| Features | Excellent Processability,Good Clarity,Good coloring,HB |
| Availabilitys | Africa & Middle East ,North America,Latin America,Asia Pacific |
| Process Methods | Injection Molding |
| Technical Data | |||
|---|---|---|---|
| MECHANICAL | Nominal value | Unit | Test method |
| Shore hardness | |||
| Shore A, 10 seconds, 23 ℃ | 59 | ASTM D2240 | |
| elastic body | Nominal value | Unit | Test method |
|---|---|---|---|
| tensile strength | |||
| Fracture, 23 ℃ | 4.50 | MPa | ASTM D412 |
| 300%应变，23℃ | 3.39 | MPa | ASTM D412 |
| Tensile strain | |||
| Fracture, 23 ℃ | 560 | % | ASTM D412 |
| tear strength | 31.5 | kN/m | ASTM D624 |
| Compression deformation | |||
| 23℃，22 hr | 33 | % | ASTM D395B |
| FLAME CHARACTERISTICS | Nominal value | Unit | Test method |
|---|---|---|---|
| Flame retardant level | |||
| 1.50 mm | HB | UL 94 |
| PHYSICAL | Nominal value | Unit | Test method |
|---|---|---|---|
| Density | 0.898 | g/cm³ | ASTM D792 |
| Shrinkage rate | |||
| MD | 0.80 to 1.2 | % | ASTM D955 |
| Apparent viscosity of melt | |||
| 200℃，11200 sec^-1 | 13.0 | Pa·s | ASTM D3835 |
| Process Conditions | |||
|---|---|---|---|
| injection | Nominal value | Unit | Test method |
| Proposed maximum recycled material ratio | 20 | % | |
| Barrel rear temperature | 177 to 216 | °C | |
| Barrel middle temperature | 182 to 221 | °C | |
| Barrel front temperature | 193 to 232 | °C | |
| Nozzle temperature | 204 to 243 | °C | |
| Mold temperature | 21 to 32 | °C | |
| Back pressure | 0.517 to 1.21 | MPa | |
| Screw speed | 75 to 125 | rpm | |
| 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 |
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