 | Manufacturer | Indicates the medical device manufacturer | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.1.1 |
 | Do Not Re-use | Indicates a medical device that is intended for one single use only NOTE: Synonyms for “Do not reuse” are “single use” and “use only once”. | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.4.2 |
 | Date of Manufacture | Indicates the date when the medical device was manufactured | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.1.3 |
 | Use-by Date | Indicates the date after which the medical device is not to be used | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.1.4 |
 | Batch Code | Indicates the manufacturer’s batch code so that the batch or lot can be identified. NOTE: Synonyms for “batch code” are “lot number”, “lot code” and “batch number”. | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.1.5 |
 | Medical Device | Indicates the item is a medical device | ISO15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.7.7 |
 | Catalogue number | Indicates the manufacturer’s catalog number so that the medical device can be identified | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.1.6 |
 | Not Made with or Absence of Natural Rubber Latex | Indicates the absence of dry natural rubber or natural rubber latex as a material of construction within the medical device or the packaging of a medical device | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. Annex B (b.2) |
 | Do Not Use if Package is Damaged and Consult Instructions for Use | Indicates a medical device that should not be used if the package has been damaged or opened and that the user should consult the instructions for use for additional information | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.2.8 |
 | Non-Sterile | Indicates a medical device that has not been subjected to a sterilization process | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.2.7 |
 | Keep Away from Sunlight | Indicates a medical device that needs protection from light sources | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.3.2 |
 | Keep Dry | Indicates a medical device that needs protection from moisture | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.3.4 |
 | Temperature Limit | Indicates the temperature limits to which the medical device can be safely exposed | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.3.7 |
 | CE Marking | CE marking of conformity means a marking by which a manufacturer indicates that a device is in conformity with the applicable requirements set out in this Regulation and other applicable Union harmonisation legislation providing for its affixing | Regulation (EU) 2017/745 | REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC |
| Reference no. Annex V |
 | Contains potential Type IV chemical allergens | For any medical glove where chemical ingredients such as accelerators, antioxidants and biocides are added during the manufacturing or already known to be present in the product and there is a residual risk of causing Type IV allergy | BS EN 455-3 | Medical gloves for single use – Part 3: Requirements and testing for biological evaluation |
| Reference no 4.6 (b) |
 | Consult Instructions for Use or Consult Electronic Instructions for Use | Indicates the need for the user to consult the instructions for use | ISO 15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.4.3 |
 | Unique Device Identifier | Indicates a carrier that contains unique device identifier information | ISO15223-1 | Medical devices — Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements |
| Reference no. 5.7.10 |
 | | Indicates a carrier that contains unique device identifier information | | |
| | | |
 | | The material used in the product is suitable for direct contact with food and beverages. | | |
| | | |
 | | Indicates a carrier that contains unique device identifier information | | |
| | | |
 | | Indicates a carrier that contains unique device identifier information | | |
| | | |
