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DIN EN ISO 5832-2

Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:1999)

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Organization: DIN
Publication Date: 1 August 2012
Status: inactive
Page Count: 10
ICS Code (Titanium and titanium alloys): 77.120.50
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40
scope:

This part of ISO 5832 specifies the characteristics of, and corresponding test methods for, unalloyed titanium for use in the manufacture of surgical implants.

Provision is made for six grades of titanium based on tensile strength.

NOTE The mechanical properties of a sample obtained from a finished product made of this metal may not necessarily comply with those specified in this part of ISO 5832.

Document History

DIN EN ISO 5832-2
July 1, 2018
Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:2018)
This document specifies the characteristics of, and corresponding test methods for, unalloyed titanium for use in the manufacture of surgical implants. Six grades of titanium based on tensile...
DIN EN ISO 5832-2
February 1, 2017
Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO/DIS 5832-2:2017); German and English version prEN ISO 5832-2:2017
A description is not available for this item.
DIN EN ISO 5832-2
August 1, 2012
Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:1999)
This part of ISO 5832 specifies the characteristics of, and corresponding test methods for, unalloyed titanium for use in the manufacture of surgical implants. Provision is made for six grades of...

References

This document references:
ASTM E112 - Standard Test Methods for Determining Average Grain Size
Published by ASTM on October 1, 2013
These test methods cover the measurement of average grain size and include the comparison procedure, the planimetric (or Jeffries) procedure, and the intercept procedures. These test methods may also...
This document references:
DIN EN ISO 6892-1 - Metallic materials - Tensile testing - Part 1: Method of test at room temperature (ISO 6892-1:2019)
Published by DIN on June 1, 2020
A description is not available for this item.
This document references:
ISO 6892-1 - Metallic materials — Tensile testing — Part 1: Method of test at room temperature
Published by ISO on November 1, 2019
This document specifies the method for tensile testing of metallic materials and defines the mechanical properties which can be determined at room temperature. NOTE Annex A contains further...
This document references:
ISO 6892-2 - Metallic materials - Tensile testing - Part 2: Method of test at elevated temperature
Published by ISO on March 1, 2018
This document specifies a method of tensile testing of metallic materials at temperatures higher than room temperature.
This document references:
ISO 7438 - Metallic materials — Bend test
Published by ISO on October 1, 2020
This document specifies a method for determining the ability of metallic materials to undergo plastic deformation in bending. This document applies to test pieces taken from metallic products, as...
This document is referenced by:
DIN EN ISO 22674 - Dentistry - Metallic materials for fixed and removable restorations and appliances (ISO 22674:2016)
Published by DIN on September 1, 2016
This International Standard classifies metallic materials that are suitable for the fabrication of dental restorations and appliances, including metallic materials recommended for use either with or...
This document is referenced by:
DIN EN ISO 13504 - Dentistry - General requirements for instruments and related accessories used in dental implant placement and treatment (ISO 13504:2012)
Published by DIN on October 1, 2012
This International Standard specifies general requirements for the manufacture of instruments and related accessories used in the placement of dental implants and further manipulations of connecting...
This document is referenced by:
DIN EN ISO 5840-3 - Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2013)
Published by DIN on June 1, 2013
This part of ISO 5840 outlines an approach for verifying/validating the design and manufacture of a transcatheter heart valve substitute through risk management. The selection of appropriate...
This document is referenced by:
DIN EN ISO 10555-6 - Intravascular catheters - Sterile and single-use catheters - Part 6: Subcutaneous implanted ports (ISO 10555-6:2015 + Amd 1:2019) (includes Amendment A1:2019)
Published by DIN on February 1, 2020
A description is not available for this item.
This document is referenced by:
VDI 5701 - Biomaterials in medicine - Classification, requirements, and applications
Published by VDI on May 1, 2018
The standard pertains to biomaterials and their use in the production of medical devices (e.g. implants) for use in the living organism, in particular, in humans and animals. Biomaterials belonging...
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