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Technical Data Sheet
Eastman Provista™ Copolymer MP001


Applications
  • Medical devices

Product Description
Eastman Provista™ Copolymer MP001 is a resin specifically developed for extrusion into profiles where aesthetics such as high clarity and gloss, coupled with design flexibility, drive demand. Compared to commonly used materials, Eastman Provista™ copolymer runs on most standard processing equipment at increased speeds. An extremely high melt strength makes the resin an excellent choice when extruding profiles into complicated shapes. In addition to profile extrusion, Eastman Provista™ copolymer is an excellent choice for extrusion of rigid tubing. This product meets the biocompatibility requirements under FDA/ISO 10993 and USP Class 6, Plastics.

This product has been GREENGUARD INDOOR AIR QUALITY CERTIFIED®.
The GREENGUARD INDOOR AIR QUALITY CERTIFIED® Mark is a registered certification mark used under license through the GREENGUARD Environmental Institute (GEI). GEI is an industry-independent, non-profit organization that oversees the GREENGUARD Certification Program. The GREENGUARD Certification Program is an industry independent, third-party testing program for low-emitting products and materials for indoor environments. For more information about GEI and to obtain printable certificates for Eastman™ Copolyesters, visit www.greenguard.org. Choose Eastman Chemical Company under the Manufacturer category and click search to display a list of our products.



Typical Properties

PropertyaTest MethodbTypical Value, Unitsc
General Properties
DensityD 792 1.27 g/cm3
Mechanical Properties
Tensile Stress @ YieldD 63850 MPa (7300 psi)
Tensile Stress @ BreakD 63829 MPa (4200 psi)
Elongation @ YieldD 6384 %
Elongation @ BreakD 638109 %
Flexural ModulusD 7902200 MPa (3.2 x 105 psi)
Flexural StrengthD 79072 MPa (10400 psi)
Rockwell Hardness, R ScaleD 785106
Izod Impact Strength, Notchedd 
     @ 23°C (73°F)D 25694 (9C/1NB) J/m (1.8 (9C/1NB) ft·lbf/in.)
     @ -40°C (-40°F)D 25652C J/m (1.0C ft·lbf/in.)
Impact Strength, Unnotchede 
     @ 23°C (73°F)D 4812NB
     @ -40°C (-40°F)D 4812NB
Impact Resistance (Puncture), Energy @ Max. Loadf 
     @ 0°C (32°F)D 376337 J (27 ft·lbf)
     @ 23°C (73°F)D 376333 J (24 ft·lbf)
     @ -40°C (-40°F)D 376341 J (30 ft·lbf)
Optical Properties
HazeD 10030.6 %
Regular TransmittanceD 100388 %
Total TransmittanceD 100390 %
Gloss 
     @ 60°D 2457171
Color, b* 
     CIELAB, Illuminant D6500, 10° ObserverD 22440.61
Thermal Properties
Deflection Temperature 
     @ 0.455 MPa (66 psi)D 64867 °C (153 °F)
     @ 1.82 MPa (264 psi)D 64862 °C (144 °F)
Vicat Softening Temperature 
     @ 1 kg loadD 152579 °C (174 °F)

aUnless noted otherwise, all tests are run at 23°C (73°F) and 50% relative humidity.
bUnless noted otherwise, the test method is ASTM.
cUnits are in SI or US customary units.
dTesting conducted using 10 standard flex bars with 20 mil notch; C = complete break; NB = nonbreak.
eNonbreak as defined by ASTM D 4812.
fTesting conducted using 10 standard 4" x 4" x 0.125" thick injection molded plaques; 100% ductile break.



Comments
Properties reported here are based on limited testing. Eastman makes no representation that the material in any particular shipment will conform exactly to the values given.

Eastman Medical Disclaimer
It is the responsibility of the medical device manufacturer ("Manufacturer") to determine the suitability of all component parts and raw materials, including any Eastman product, used in its final product in order to ensure safety and compliance with requirements of the United States Food and Drug Administration (FDA) or other international regulatory agencies.

Eastman Chemical Company products have not been designed for nor are they promoted for end uses that would be categorized by either the United States FDA or by the International Standards Organization (ISO) as implant devices. Eastman products are not intended for use in the following applications: (1) in any bodily implant applications for greater than 30 days, based on FDA-Modified ISO-10993, Part 1 “Biological Evaluation of Medical Devices” tests (including any cosmetic, reconstructive or reproductive implant applications); (2) in any cardiac prosthetic device application, regardless of the length of time involved, including, without limitation, pacemaker leads and devices, artificial hearts, heart valves, intra-aortic balloons and control systems, and ventricular bypass assisted devices, or (3) as any critical component in any medical device that supports or sustains human life.

Eastman Chemical Company products offered for the medical market have met selected FDA-Modified ISO-10993, Part 1 “Biological Evaluation of Medical Devices” tests with human tissue contact time of 30 days or less. The tests include: cytotoxicity, sensitization, irritation or intracutaneous reactivity, systemic toxicity (acute), subchronic toxicity (sub-acute), implantation, hemocompatibility. The Manufacturer is responsible for the biological evaluation of the finished medical device.

The suitability of an Eastman Product in a given end-use environment is dependent upon various conditions including, without limitation, chemical compatibility, temperature, part design, sterilization method, residual stresses, and external loads. It is the responsibility of the Manufacturer to evaluate its final product under actual end-use requirements and to adequately advise and warn purchasers and users thereof.


Eastman and its marketing affiliates shall not be responsible for the use of this information, or of any product, method, or apparatus mentioned, and you must make your own determination of its suitability and completeness for your own use, for the protection of the environment, and for the health and safety of your employees and purchasers of your products. No warranty is made of the merchantability of fitness of any product, and nothing herein waives any of the Seller's conditions of sale.


2/28/2018 11:35:39 AM