Knowde Enhanced TDS
Identification & Functionality
- Additives Included
- Chemical Family
- Polymer Name
- Plastics & Elastomers Functions
- Technologies
- Product Families
Features & Benefits
- Labeling Claims
Applications & Uses
- Applications
- Plastics & Elastomers Processing Methods
- Applications
- Monofilaments
- Stretched tapes
- Films for lamination
- Co-extruded films
- Drip-bag over pouches
- Processing Conditions
Typical processing conditions Extrusion Film Extrusion Feed Zone (°C) 170 170 Die (°C) 250 - 260 210 - 220 Melt Temp (°C) 210 - 250 190 - 240 - Safripol Medical Application Policy
Safripol will not knowingly sell or sample any product or service (“Product”) into any commercial or developmental application that is intended for:
a. permanent (Long term) contact with internal body fluids or internal body tissues. Long term is a use which exceeds 72 continuous hours.
b. use in cardiac prosthetic devices regardless of the length of time involved; (Cardiac prosthetic devices include, but are not limited to, pacemaker leads and devices, artificial hearts, heart valves, intra-aortic balloons and control systems, and ventricular bypass assisted devices);
c. use as a critical component in medical devices that support or sustain human life; or
d. use specifically by pregnant women or in applications designed specifically to promote or interfere with human reproduction.
Additionally, all Products intended for use in pharmaceutical applications, other than pharmaceutical packaging, must pass the current Pharmaceutical Liability Guidelines.
● New business opportunities require a business assessment prior to sale or sampling of Safripol products.
● Authorized distributors and resellers will adhere to this medical policy.
● Safripol does not endorse or claim suitability of their products for specific medical applications. It is the responsibility of the medical device or pharmaceutical manufacturer to determine that the Safripol product is safe, lawful, and technically suitable for the intended use.
SAFRIPOL MAKES NO WARRANTIES, EXPRESS OR IMPLIED, CONCERNING THE SUITABILITY OF ANY SAFRIPOL PRODUCT FOR USE IN MEDICAL APPLICATIONS.
Properties
- Physical Properties
- Mechanical Properties
- Thermal Properties
| Value | Units | Test Method / Conditions | |
| Melt Flow Rate (190 °C/ 5 kg) | 1.9 | g/10min | ISO 1133 |
| Melt Flow Rate (190 °C/ 2.16 kg) | 0.4 | g/10min | ISO 1133 |
| Density | 0.946 | g/cm3 | ISO 1183 |
| Viscosity Number | 270 | Shore D | ISO 1628-3 |
| Spiral Flow Test | 32 | MPa | Internal |
| Value | Units | Test Method / Conditions | |
| Hardness | 60 | Shore D | ISO 868 |
| Tensile Yield | 21 | MPa | ISO 527 |
| Ultimate Tensile | 33 | MPa | ISO 527 |
| Ultimate Elongation | min. 600 | % | ISO 527 |
| Flexural Modulus (3.5% Deflection) | 17 | MPa | ISO 178 |
| Charpy Notched Impact Strength (23 °C) | 15 | kJ/m2 | ISO 179 |
| Charpy Notched Impact Strength (-30 °C) | 8 | kJ/m2 | ISO 179 |
| Value | Units | Test Method / Conditions | |
| Vicat Softening Point B (50N) | 73 | °C | ISO 306B |
| Crystalline Melting Range | 130-133 | °C | ISO 3146-85 |
Regulatory & Compliance
- Certifications & Compliance
- Food Contact Compliance
Safrene® F 7740F2 High Density Polyethylene Resin should comply with Commission Regulation (EU) No 10/2011 and with U.S. FDA 21 CFR 177.1520(c)3.2a food contact regulations when used unmodified and processed according to good manufacturing practices for food contact applications. The purchaser remains responsible for determining whether the use complies with all relevant regulations.