Röchling (Roechling) SUSTASON PPSU Plate and Rod

Medical-grade materials featuring excellent sterilizability and tested on semi-finished products for USP Class VI and ISO 10993 compliance. These materials boast a high heat deflection temperature, are highly impact resistant, and offer excellent chemical resistance. 

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‧Medical engineering

Data sheet Product Handling Colored FDA Compliance


Material

Material

  • Very good sterilizability
  • USP VI and ISO 10993 tested on semi-finished product
  • High heat deflection temperature
  • Highly impact resistant
  • Excellent chemical resistance
  • Medical grade material
 

Plate Size

Standard Dimension
Width & Depth Thickness
Width & Depth 2,000 x 620 6 - 100
3,000 x 620
 Other sizes Please ask by phone or on-line inquiry.  
Unit:mm
 

Rod Size

Standard Dimension
Length Diameter
Standard Dimension 1,000 / 2,000 / 3,000 Ø 6 - 100
 Other sizes Please ask by phone or on-line inquiry. 
Unit:mm
 
Color

Color

  • Black
  • Blue
  • Bone
  • Brown
  • Green
  • Grey
  • Natural
  • Red
  • Rust
  • Yellow
 

Röchling

Germany's Rochling stands at the forefront of industrial plastic semi-finished product manufacturing, producing a wide array of plastic products utilized across various industries. Specializing in the manufacture and sale of Polystone® thermoplastic sheet products, Rochling offers materials such as Polystone®M UHMW-PE, Polystone®G HDPE, HDPE piping, PVC, PEEK, and Polystone®P Polypropylene. These materials are available in thicknesses ranging from 3/8 to 4 inches, with sizes customizable to meet any client requirement, from the smallest to virtually unlimited dimensions. Additionally, Rochling produces Durostone®CHP, a fiberglass-reinforced plastic used in the assembly and soldering operations of printed circuit boards.
Unique in the United States, Rochling's engineering plastics division is the sole supplier of plastics for medical devices to hold the ISO 13485:2003 certification. This certification signifies that a company's management system fully meets the comprehensive requirements in the design and manufacture of medical devices, highlighting:

  • The capability to ensure product safety.
  • Risk management proficiency.
  • Traceable inspection procedures.
  • Rigorous documentation and verification processes.
  • Effective corrective and preventive validation.
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