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NATO - AAITP-02 - NATO ASSET TRACKING SHIPPING LABEL AND ASSOCIATED SYMBOLOGIES - ED A; VER 1 Organization: NATO
Date: 2012-10-29
Description: Where information is bar coded using GS1-128 bar codes, the information title is to be printed in clear in the human readable portion of the label. The recommended sizes for these labels are ISO standard paper size A5, (148 x 210 mm), or US 4 x 6 inches.
DS/EN 606 - BAR CODING - TRANSPORT AND HANDLING LABELS FOR STEEL PRODUCTS Organization: DS
Date: 2005-04-11
Description: This document specifies the requirements for labels containing human readable and bar coded information for fixing to steel products for the purpose of despatch, transport, and reception in accordance with the requirements of ISO 15394. Data elements are specified together with their status, location on the label, the appropriate data identifier and choice of bar code symbology.
TSE - TS ISO 12891-1 - RETRIEVAL AND ANALYSIS OF SURGICAL IMPLANTS - PART 1: RETRIEVAL AND HANDLING Organization: TSE
Date: 2016-12-09
Description: In particular, it specifies the essential stepsto be followed for the safe and proper obtaining of the clinicalhistory, pre-explantation checks and examinations, collection,labelling, cleaning, decontamination, documentation, packing andshipping. This part of ISO 12891 also provides guidance oninfection control.
DS/ISO 12891-1 - RETRIEVAL AND ANALYSIS OF SURGICAL IMPLANTS - PART 1: RETRIEVAL AND HANDLING Organization: DS
Date: 2015-08-14
Description: ISO 12891-1:2015 specifies the method to be followed for the retrieval and handling of surgical implants and associated tissues and fluids.
ISO - ISO 12891-1 - RETRIEVAL AND ANALYSIS OF SURGICAL IMPLANTS - PART 1: RETRIEVAL AND HANDLING - THIRD EDITION Organization: ISO
Date: 2015-07-01
Description: In particular, it specifies the essential steps to be followed for the safe and proper obtaining of the clinical history, pre-explantation checks and examinations, collection, labelling, cleaning, decontamination, documentation, packing and shipping. This part of ISO 12891 also provides guidance on infection control.
ISO - ISO 29061-4 - ROAD VEHICLES - METHODS AND CRITERIA FOR USABILITY EVALUATION OF CHILD RESTRAINT SYSTEMS AND THEIR INTERFACE WITH VEHICLE ANCHORAGE SYSTEMS - PART 4: SECURING OF CHILD IN CHILD RESTRAINT SYSTEM AND DAILY HANDLING ASPECTS - FIRST EDITION Organization: ISO
Date: 2017-12-01
Description: The document provides criteria for judgement of: — ease of availability of instructions; — clarity of instruction manual and labelling; and — the ease of use of design related features of the CRS related to securing the child or child dummy in a CRS installed in vehicle.
DSF/PREN ISO 12870 - OPHTHALMIC OPTICS - SPECTACLE FRAMES - REQUIREMENTS AND TEST METHODS (ISO/DIS 12870:2015) Organization: DS
Description: It applies to devices intended for patient or caregiver administration of medicinal products to humans. This part of ISO 11608 covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
DSF/FPREN ISO 12870 - OPHTHALMIC OPTICS - SPECTACLE FRAMES - REQUIREMENTS AND TEST METHODS (ISO/FDIS 12870:2016) Organization: DS
Description: It applies to devices intended for patient or caregiver administration of medicinal products to humans. This part of ISO 11608 covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
DIN EN ISO 11608-7 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 7: ACCESSIBILITY FOR PERSONS WITH VISUAL IMPAIRMENT (ISO 11608-7:2016) Organization: DIN
Date: 2017-10-01
Description: This part of ISO 11608 covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
DSF/FPREN ISO 11608-7 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE – REQUIREMENTS AND TEST METHODS – PART 7: ACCESSIBILITY FOR PERSONS WITH VISUAL IMPAIRMENT (ISO 11608-7:2016) Organization: DS
Description: It covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
DS/EN ISO 11608-7 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE – REQUIREMENTS AND TEST METHODS – PART 7: ACCESSIBILITY FOR PERSONS WITH VISUAL IMPAIRMENT (ISO 11608-7:2016) Organization: DS
Date: 2017-08-07
Description: It covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
DS/ISO TR 80002-2 - MEDICAL DEVICE SOFTWARE – PART 2: VALIDATION OF SOFTWARE FOR MEDICAL DEVICE QUALITY SYSTEMS Organization: DS
Date: 2017-06-19
Description: ISO/TR 80002-2:2017(E) applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485.
ISO - ISO TR 80002-2 - MEDICAL DEVICE SOFTWARE - PART 2: VALIDATION OF SOFTWARE FOR MEDICAL DEVICE QUALITY SYSTEMS - FIRST EDITION Organization: ISO
Date: 2017-06-01
Description: This document applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485.
AAMI TIR80002-2 - MEDICAL DEVICE SOFTWARE - PART 2: VALIDATION OF SOFTWARE FOR MEDICAL DEVICE QUALITY SYSTEMS Organization: AAMI
Date: 2017-01-01
Description: This document applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485.
DS/ISO 18616-1 - TRANSPORT PACKAGING – REUSABLE, RIGID PLASTIC DISTRIBUTION BOXES – PART 1: GENERAL PURPOSE APPLICATION Organization: DS
Date: 2016-11-14
Description: This document defines the main types of rigid plastic distribution boxes, dimensions, safety, designation, marking and labeling. ISO 18616-1:2016 is designed for general purpose applications in a returnable transport system.
CEN - EN ISO 11608-7 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 7: ACCESSIBILITY FOR PERSONS WITH VISUAL IMPAIRMENT Organization: CEN
Date: 2017-08-01
Description: This part of ISO 11608 covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
ISO - 11608-7 - NEEDLE-BASED INJECTION SYSTEMS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS - PART 7: ACCESSIBILITY FOR PERSONS WITH VISUAL IMPAIRMENT - FIRST EDITION Organization: ISO
Date: 2016-08-01
Description: This part of ISO 11608 covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use.
ISO - 18616-1 - TRANSPORT PACKAGING - REUSABLE, RIGID PLASTIC DISTRIBUTION BOXES - PART 1: GENERAL PURPOSE APPLICATION - FIRST EDITION Organization: ISO
Date: 2016-11-15
Description: For automotive industry application, ISO 19709-1, ISO/TS 19709-2 and ISO/TS 19709-3 can be referenced
TSE - TS EN ISO 11334-4 - WALKING AIDS MANIPULATED BY ONE ARM- REQUIREMENTS AND TEST METHODS- PART 4: WALKING STICKS WITH THREE OR MORE LEGS Organization: TSE
Date: 2013-10-09
Description: It also gives the requirements relating to safety,ergonomics, performance, marking and labelling. The requirementsand tests are based on everyday usage of walking sticks with threeor more legs, manufactured for a user weight (mass) of not lessthan 35 kg.
DS/EN ISO 11469 - PLASTICS – GENERIC IDENTIFICATION AND MARKING OF PLASTICS PRODUCTS Organization: DS
Date: 2016-10-24
Description: Generic identification of the plastics is provided by the symbols and abbreviated terms given in ISO 1043?1, ISO 1043?2, ISO 1043?3 and ISO 1043?4. NOTE 2 – If more detailed information for material identification is needed, additional marking of plastics products can be applied as defined in the appropriate product standard.

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