Customer Support: 131 242

  • There are no items in your cart
We noticed you’re not on the correct regional site. Switch to our AMERICAS site for the best experience.
Dismiss alert

ISO 5832-4:2014

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Implants for surgery — Metallic materials — Part 4: Cobalt-chromium-molybdenum casting alloy
Available format(s)

Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users

Superseded date

03-04-2024

Language(s)

French, English

Published date

09-09-2014

ISO 5832-4:2014 specifies the characteristics of, and corresponding test methods for, cobalt-chromium-molybdenum casting alloy for use in the manufacture of surgical implants.

Committee
ISO/TC 150/SC 1
DevelopmentNote
Supersedes ISO/DIS 5832-4. (09/2014)
DocumentType
Standard
Pages
2
PublisherName
International Organization for Standardization
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
AS ISO 5832.4:2015 Identical
NF ISO 5832-4 : 2014 Identical
NEN ISO 5832-4 : 2014 Identical
DIN ISO 5832-4:2015-12 Identical
BS ISO 5832-4:2014 Identical
DS ISO 5832-4 : 2014 Identical
GOST R ISO 5832-4 : 2011 Identical
UNI 9763-4 : 1990 Similar to
BIS IS 5347-5 : 2000 Identical
AS 2320.4-1979 Identical
CSA ISO 5832-4 : 0 Identical

ASTM F 2068 : 2015 : REDLINE Standard Specification for Femoral Prostheses—Metallic Implants
UNE-EN ISO 16061:2015 Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015)
BS ISO 12891-2:2014 Retrieval and analysis of surgical implants Analysis of retrieved surgical implants
ASTM F 2887 : 2017 : REDLINE Standard Specification for Total Elbow Prostheses
BS EN ISO 10993-6:2016 Biological evaluation of medical devices Tests for local effects after implantation
BS EN 12010:1998 Non-active surgical implants. Joint replacement implants. Particular requirements
I.S. EN ISO 10993-6:2016 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016)
DIN EN ISO 16061:2015-09 Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015)
ANSI/AAMI/ISO 10993-6:2016 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION
ASTM F 3018 : 2017 Standard Guide for Assessment of Hard-on-Hard Articulation Total Hip Replacement and Hip Resurfacing Arthroplasty Devices
14/30261590 DC : 0 BS EN ISO 10993-6 - BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION
13/30242622 DC : 0 BS ISO 12891-2 - RETRIEVAL AND ANALYSIS OF SURGICAL IMPLANTS - PART 2: ANALYSIS OF RETRIEVED SURGICAL IMPLANTS
CSA ISO 10993-6 : 1997(R2009) BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION
ASTM F 3047M : 2015 Standard Guide for High Demand Hip Simulator Wear Testing of Hard-on-hard Articulations
ISO 16061:2015 Instrumentation for use in association with non-active surgical implants General requirements
BS EN 30993-6:1995 Biological evaluation of medical devices Tests for local effects after implantation
EN ISO 10993-6:2016 Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
BS EN ISO 16061:2015 Instrumentation for use in association with non-active surgical implants. General requirements
ISO 12891-2:2014 Retrieval and analysis of surgical implants Part 2: Analysis of retrieved surgical implants
I.S. EN ISO 16061:2015 INSTRUMENTATION FOR USE IN ASSOCIATION WITH NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 16061:2015)
DIN EN ISO 10993-6:2009-08 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016)
ISO 10993-6:2016 Biological evaluation of medical devices Part 6: Tests for local effects after implantation
EN ISO 16061:2015 Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015)
DIN EN ISO 10993-6:2017-09 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016)

ISO 6892-1:2016 Metallic materials Tensile testing Part 1: Method of test at room temperature

View more information
$118.72
Including GST where applicable

Access your standards online with a subscription

Features

  • Simple online access to standards, technical information and regulations.

  • Critical updates of standards and customisable alerts and notifications.

  • Multi-user online standards collection: secure, flexible and cost effective.

Need help?
Call us on 131 242, then click here to start a Screen Sharing session
so we can help right away! Learn more