Versaflex™ CL E90

About
Versaflex™ CL E90 is an exceptional clarity, high performance and autoclavable solution ideal for healthcare and food packaging. Versaflex™ CL E90 is also formulated without the use of plasticizers. New Product. Commercial specifications have not been established. Flexible Formulated without Plasticizers High Clarity&&

Product Description
SupplierPolyone
GenericTPE
Material StatusCommercial: Active
FeaturesGood Clarity,Good flexibility
AvailabilitysAfrica & Middle East ,North America,Latin America,Asia Pacific
Process MethodsExtrusion

Technical Data
MECHANICALNominal valueUnitTest method
Shore hardness
Shore A, 10 seconds90 ASTM D2240

filmNominal valueUnitTest method
Oxygen permeability ASTM D3985
21℃,120 µm280cm³·mm/m²/atm/24 hrASTM D3985
21℃,1800 µm260cm³·mm/m²/atm/24 hrASTM D3985
Oxygen transfer rate ASTM D3985
21℃,120 µm2300cm³/m²/24 hrASTM D3985
21℃,1800 µm140cm³/m²/24 hrASTM D3985

elastic bodyNominal valueUnitTest method
tensile strength ASTM D412
Fracture, 23 ℃12.6MPaASTM D412
100% strain, 23 ℃6.89MPaASTM D412
300% Strain, 73°F8.51MPaASTM D412
Tensile strain
Fracture, 23 ℃570%ASTM D412
Compression deformation ASTM D395B
22℃,22 hr27%ASTM D395B
70℃,22 hr67%ASTM D395B
100℃,22 hr73%ASTM D395B

PHYSICALNominal valueUnitTest method
Density0.898g/cm³ASTM D792
Apparent viscosity of melt ASTM D3835
200℃,1340 sec^-1162Pa·sASTM D3835
200℃,11200 sec^-134.0Pa·sASTM D3835

Process Conditions
ExtrusionNominal valueUnitTest method
Melt temperature182 to 204°C
Nozzle temperature171 to 199°C

Notes
1. Please contact GLS Thermoplastic Elastomers for a copy of the FDA compliance letter.
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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