Abstract
This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available globally and need to meet different regulatory requirements.
These symbols can be used on the medical device itself, on its packaging or in the accompanying information. The requirements of this document are not intended to apply to symbols specified in other standards.
General information
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Status: PublishedPublication date: 2021-07
Corrected version (fr): 2022-02Stage: International Standard published [60.60] -
Edition: 4Number of pages: 36
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Technical Committee :ISO/TC 210
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Amendments
Amendments are issued when it is found that new material may need to be added to an existing standardization document. They may also include editorial or technical corrections to be applied to the existing document.
Amendment 1
Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific
Edition 2025
ISO 15223-1:2021/Amd 1:2025
86270
CHF
18
Convert Swiss francs (CHF) to your currency
Life cycle
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Previously
WithdrawnISO 15223-1:2016
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Now
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00
Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Amendments
Provide additional content; available for purchase; not included in the text of the existing standard.PublishedISO 15223-1:2021/Amd 1:2025
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00