About |
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Versaflex™ HC MT555 is an easy processing material designed for applications where FDA compliance and medical testing is required. Excellent Colorability Soft Touch&& |
Product Description | |
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Supplier | Polyone |
Generic | TPE |
Material Status | Commercial: Active |
Features | Excellent Processability,Good coloring |
Availabilitys | Africa & Middle East ,North America,Latin America,Asia Pacific |
Process Methods | Injection Molding |
Technical Data | |||
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MECHANICAL | Nominal value | Unit | Test method |
Shore hardness | |||
Shore A, 10 seconds | 54 | ASTM D2240 |
elastic body | Nominal value | Unit | Test method |
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tensile strength | ASTM D412 | ||
Fracture, 23 ℃ | 6.38 | MPa | ASTM D412 |
100% strain, 23 ℃ | 1.74 | MPa | ASTM D412 |
300% Strain, 73°F | 3.31 | MPa | ASTM D412 |
Tensile strain | |||
Fracture, 23 ℃ | 630 | % | ASTM D412 |
Compression deformation | |||
23℃,22 hr | 20 | % | ASTM D395B |
PHYSICAL | Nominal value | Unit | Test method |
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Density | 0.888 | g/cm³ | ASTM D792 |
Shrinkage rate | |||
MD | 1.6 to 2.2 | % | ASTM D955 |
Apparent viscosity of melt | ASTM D3835 | ||
200℃,1340 sec^-1 | 73.0 | Pa·s | ASTM D3835 |
200℃,11200 sec^-1 | 13.1 | Pa·s | ASTM D3835 |
Process Conditions | |||
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injection | Nominal value | Unit | Test method |
Extrusion | Nominal value | Unit | Test method |
Proposed maximum recycled material ratio | 20 | % | |
Barrel rear temperature | 166 to 182 | °C | |
Barrel middle temperature | 182 to 204 | °C | |
Barrel front temperature | 188 to 210 | °C | |
Nozzle temperature | 188 to 210 | °C | |
Processing (melt) temperature | 193 to 221 | °C | |
Mold temperature | 16 to 27 | °C | |
Back pressure | 0.00 to 0.552 | MPa | |
Screw speed | 80 to 120 | rpm | |
Melt temperature | 193 to 204 | °C | |
Nozzle temperature | 193 to 204 | °C |
Notes |
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1. Please contact GLS Thermoplastic Elastomers for the specific FDA compliance letter on this product. |
2. 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 |
3. Typical properties: these are not to be construed as specifications. |
4. Die C |
5. 2 hr |
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