EN 868-5 包裝材料之熱能自封袋與塑膠薄膜
Instron® 2712-04x Series Pneumatic grips, packed with features to enhance gripping performance, usability, and operator safety.
- 0.7 MB
Screw side-action grips provide a very simple and efficient method for holding test specimens in a wide range of applications. The dual - acting design of 2710-100 series grips means that jaw faces can be adjusted to accommodate different specimen thicknesses. This ensures that the line of tensile force remains concentric with the grip body. They can be equipped with a selection of interchangeable grip jaw faces in various sizes and choice of surfaces including smooth ground, rubber-coated and serrated. Line contact and special coated faces are also available.The unique ‘snap-on’ jaw face attachment makes changing faces extremely quick and simple.
- 1.3 MB
5900 Universal Testing Systems are engineered for precision, built for durability, and offer the flexibility for changing requirements. They are designed with standard and optional features that increase testing efficiency and improve the testing experience for the operator. A wide range of models are available for testing capacities from < 100N up to 600kN.
- 6.8 MB
Instron 3300 Series Universal Testing Systems for Tensile, Compression, Bend, and other material property tests.
- 2.2 MB
Bluehill Universal Software is built from the ground-up for touch interaction and an intuitive user experience. Discover simpler and smarter testing with features such as pre-loaded test methods, QuickTest in seconds, enhanced data exporting: and Instron Connect – a new feature that provides a direct communication link to Service. Users of previous versions of software such as Bluehill 2 and Bluehill 3 can easily upgrade to the newest version of Bluehill.
- 2.6 MB
For Medical Device and Pharmaceutical companies, records management compliance with FDA 21 CFR § 11 is non-negotiable. ComplianceBuilder™ (CB) is a stand-alone, add-on compliance solution that can be integrated with Instron’s Bluehill® Software to provide features necessary to meet the latest FDA 21 CFR § 11 regulations.
- 0.5 MB