Versaflex™ OM 1040X-1

About
The Versaflex™ OM 1040X-1 is a medical compliant overmolding TPE with very good adhesion to PC or ABS-based plastics. Good Surface Aesthetics Rubbery Feel Soft Touch Very Good Bond to PC, ABS, PC/ABS&&

Product Description
SupplierPolyone
GenericTPE
Material StatusCommercial: Active
FeaturesExcellent Processability,Good surface appearance,Good coloring
AvailabilitysAfrica & Middle East ,North America,Latin America,Asia Pacific
Process MethodsInjection Molding

Technical Data
MECHANICALNominal valueUnitTest method
Shore hardness
Shore A, 10 seconds42 ASTM D2240

elastic bodyNominal valueUnitTest method
tensile strength ASTM D412
Fracture, 23 ℃3.47MPaASTM D412
100% strain, 23 ℃1.24MPaASTM D412
300% Strain, 73°F2.08MPaASTM D412
Tensile strain
Fracture, 23 ℃580%ASTM D412
tear strength17.5kN/mASTM D624
Compression deformation
23℃,22 hr22%ASTM D395B

PHYSICALNominal valueUnitTest method
Density0.918g/cm³ASTM D792
Melt Flow Rate ASTM D1238
190℃,2.16kg9.0g/10minASTM D1238
200℃,5.0kg16g/10minASTM D1238
Shrinkage rate
MD2.0 to 2.6%ASTM D955
Apparent viscosity of melt
200℃,11200 sec^-111.7Pa·sASTM D3835

Process Conditions
injectionNominal valueUnitTest method
Proposed maximum recycled material ratio20%
Barrel rear temperature166 to 188°C
Barrel middle temperature182 to 199°C
Barrel front temperature188 to 204°C
Nozzle temperature193 to 216°C
Processing (melt) temperature188 to 210°C
Mold temperature21 to 32°C
Back pressure0.00 to 0.862MPa
Screw speed75 to 125rpm

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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