Annex 6 – Information to be submitted upon the registration of devices and economic operators in accordance with Articles 29(4) and 31; core data elements to be provided to the UDI database together with the UDI-DI in accordance with Articles 28 and 29;and the UDI system

Part A

INFORMATION TO BE SUBMITTED UPON THE REGISTRATION OF DEVICES AND ECONOMIC OPERATORS IN ACCORDANCE WITH ARTICLES 29(4) AND 31

Manufacturers or, when applicable, authorised representatives, and, when applicable, importers shall submit the information referred to in Section 1 and shall ensure that the information on their devices referred to in Section 2 is complete, correct and updated by the relevant party.

1. 1.Information relating to the economic operator
2. 1.1.type of economic operator(manufacturer, authorised representative, or importer),
3. 1.2.name, address and contact details of the economic operator,
4. 1.3.where submission of information is carried out by another person on behalf of any of the economic operators mentioned under Section 1.1, the name, address and contact details of that person,
5. 1.4.name address and contact details of the person or persons responsible for regulatory compliance referred to in Article 15.
6. 2.Information relating to the device
7. 2.1.Basic UDI-DI,
8. 2.2.type, number and expiry date of the certificate issued by the notified body and the name or identification number of that notified body and the link to the information that appears on the certificate and was entered by the notified body in the electronic system on notified bodies and certificates,
9. 2.3.Member State in which the device is to or has been placed on the market in the Union,
10. 2.4.in the case of class IIa, class IIb or class III devices: Member States where the device is or is to be made available,
11. 2.5.risk class of the device,
12. 2.6.reprocessed single-use device (y/n),
13. 2.7.presence of a substance which, if used separately, may be considered to be a medicinal product and name of that substance,
14. 2.8.presence of a substance which, if used separately, may be considered to be a medicinal product derived from human blood or human plasma and name of this substance,
15. 2.9.presence of tissues or cells of human origin, or their derivatives (y/n),
16. 2.10.presence of tissues or cells of animal origin, or their derivatives, as referred to in Regulation (EU) No 722/2012 (y/n),
17. 2.11.where applicable, the single identification number of the clinical investigation or investigations conducted in relation to the device or a link to the clinical investigation registration in the electronic system on clinical investigations,
18. 2.12.in the case of devices listed in Annex XVI, specification as to whether the intended purpose of the device is other than a medical purpose,
19. 2.13.in the case of devices designed and manufactured by another legal or natural person as referred in Article 10(15), the name, address and contact details of that legal or natural person,
20. 2.14.in the case of class III or implantable devices, the summary of safety and clinical performance,
21. 2.15.status of the device (on the market, no longer placed on the market, recalled, field safety corrective action initiated).

Part B

CORE DATA ELEMENTS TO BE PROVIDED TO THE UDI DATABASE TOGETHER WITH THE UDI-DI IN ACCORDANCE WITH ARTICLES 28 AND 29

The manufacturer shall provide to the UDI database the UDI-DI and all of the following information relating to the manufacturer and the device:

1. 1.quantity per package configuration,
2. 2.the Basic UDI-DI as referred to in Article 29 and any additional UDI-DIs,
3. 3.the manner in which production of the device is controlled (expiry date or manufacturing date, lot number, serial number),
4. 4.if applicable, the unit of use UDI-DI (where a UDI is not labelled on the device at the level of its unit of use, a ‘unit of use’ DI shall be assigned so as to associate the use of a device with a patient),
5. 5.name and address of the manufacturer (as indicated on the label),
6. 6.the SRN issued in accordance with Article 31(2),
7. 7.if applicable, name and address of the authorised representative (as indicated on the label),
8. 8.the medical device nomenclature code as provided for in Article 26,
9. 9.risk class of the device,
10. 10.if applicable, name or trade name,
11. 11.if applicable, device model, reference, or catalogue number,
12. 12.if applicable, clinical size (including volume, length, gauge, diameter),
13. 13.additional product description (optional),
14. 14.if applicable, storage and/or handling conditions (as indicated on the label or in the instructions for use),
15. 15.if applicable, additional trade names of the device,
16. 16.labelled as a single-use device (y/n),
17. 17.if applicable, the maximum number of reuses,
18. 18.device labelled sterile (y/n),
19. 19.need for sterilisation before use (y/n),
20. 20.containing latex (y/n),
21. 21.where applicable, information labelled in accordance with Section 10.4.5 of Annex I,
22. 22.URL for additional information, such as electronic instructions for use (optional),
23. 23.if applicable, critical warnings or contra-indications,
24. 24.status of the device (on the market, no longer placed on the market, recalled, field safety corrective action initiated).

Part C

THE UDI SYSTEM

1. 1.Definitions

   Automatic identification and data capture (‘AIDC’)

   AIDC is a technology used to automatically capture data. AIDC technologies include bar codes, smart cards, biometrics and RFID.

   Basic UDI-DI

   The Basic UDI-DI is the primary identifier of a device model. It is the DI assigned at the level of the device unit of use. It is the main key for records in the UDI database and is referenced in relevant certificates and EU declarations of conformity.

   Unit of Use DI

   The Unit of Use DI serves to associate the use of a device with a patient in instances in which a UDI is not labelled on the individual device at the level of its unit of use, for example in the event of several units of the same device being packaged together.

   Configurable device

   A configurable device is a device that consists of several components which can be assembled by the manufacturer in multiple configurations. Those individual components may be devices in themselves.

   Configurable devices include computed tomography (CT) systems, ultrasound systems, anaesthesia systems, physiological Monitoring systems, radiology information systems (RIS).

   Configuration

   Configuration is a combination of items of equipment, as specified by the manufacturer, that operate together as a device to achieve an intended purpose. The combination of items may be modified, adjusted or customized to meet specific needs.

   Configurations include inter alia:

   • gantries, tubes, tables, consoles and other items of equipment that can be configured/combined to deliver an intended function in computed tomography.
   • ventilators, breathing circuits, vaporizers combined to deliver an intended function in anaesthesia.

   UDI-DI

   The UDI-DI is a unique numeric or alphanumeric code specific to a model of device and that is also used as the ‘access key’ to information stored in a UDI database.

   Human Readable Interpretation (‘HRI’)

   HRI is a legible interpretation of the data characters encoded in the UDI carrier.

   Packaging levels

   Packaging levels means the various levels of device packaging that contain a defined quantity of devices, such as a carton or case.

   UDI-PI

   The UDI-PI is a numeric or alphanumeric code that identifies the unit of device production.

   The different types of UDI-PIs include serial number, lot number, software identification and manufacturing or expiry date or both types of date.

   Radio Frequency Identification RFID

   RFID is a technology that uses communication through the use of radio waves to exchange data between a reader and an electronic tag attached to an object, for the purpose of identification.

   Shipping containers

   A shipping container is a container in relation to which traceability is controlled by a process specific to logistics systems.

   Unique Device Identifier (‘UDI’)

   The UDI is a series of numeric or alphanumeric characters that is created through a globally accepted device identification and coding standard. It allows the unambiguous identification of a specific device on the market. The UDI is comprised of the UDI-DI and the UDI-PI.

   The word ‘Unique’ does not imply serialisation of individual production units.

   UDI carrier

   The UDI carrier is the means of conveying the UDI by using AIDC and, if applicable, its HRI.

   UDI carriers include, inter alia, ID/linear bar code, 2D/Matrix bar code, RFID.

2. 2.General requirements
3. 2.1.The affixing of the UDI is an additional requirement — it does not replace any other marking or labelling requirements laid down in Annex I to this Regulation.
4. 2.2.The manufacturer shall assign and maintain unique UDIs for its devices.
5. 2.3.Only the manufacturer may place the UDI on the device or its packaging.
6. 2.4.Only coding standards provided by issuing entities designated by the Commission pursuant to Article 27(2) may be used.
7. 3.The UDI
8. 3.1.A UDI shall be assigned to the device itself or its packaging. Higher levels of packaging shall have their own UDI.
9. 3.2.Shipping containers shall be exempted from the requirement in Section 3.1. By way of example, a UDI shall not be required on a logistics unit; where a healthcare provider orders multiple devices using the UDI or model number of individual devices and the manufacturer places those devices in a container for shipping or to protect the individually packaged devices, the container (logistics unit) shall not be subject to UDI requirements.
10. 3.3.The UDI shall contain two parts: a UDI-DI and a UDI-PI.
11. 3.4.The UDI-DI shall be unique at each level of device packaging.
12. 3.5.If a lot number, serial number, software identification or expiry date appears on the label, it shall be part of the UDI-PI. If there is also a manufacturing date on the label, it does not need to be included in the UDI-PI. If there is only a manufacturing date on the label, this shall be used as the UDI-PI.
13. 3.6.Each component that is considered to be a device and is commercially available on its own shall be assigned a separate UDI unless the components are part of a configurable device that is marked with its own UDI.
14. 3.7.Systems and procedure packs as referred to in Article 22 shall be assigned and bear their own UDI.
15. 3.8.The manufacturer shall assign the UDI to a device following the relevant coding standard.
16. 3.9.A new UDI-DI shall be required whenever there is a change that could lead to misidentification of the device and/or ambiguity in its traceability; in particular, any change of one of the following UDI database data elements shall require a new UDI-DI:
    1. name or trade name,
    2. device version or model,
    3. labelled as single use,
    4. packaged sterile,
    5. need for sterilization before use,
    6. quantity of devices provided in a package,
    7. critical warnings or contra-indications: e.g. containing latex or DEHP.
17. 3.10.Manufacturers that repackage and/or relabel devices, with their own label shall retain a record of the original device manufacturer’s UDI.
18. 4.UDI carrier
19. 4.1.The UDI carrier (AIDC and HRI representation of the UDI) shall be placed on the label or on the device itself and on all higher levels of device packaging. Higher levels do not include shipping containers.
20. 4.2.In the event of there being significant space constraints on the unit of use packaging, the UDI carrier may be placed on the next higher packaging level.
21. 4.3.For single-use devices of classes I and IIa packaged and labelled individually, the UDI carrier shall not be required to appear on the packaging but it shall appear on a higher level of packaging, e.g. a carton containing several individually packaged devices. However, when the healthcare provider is not expected to have access, in cases such as in home healthcare settings, to the higher level of device packaging, the UDI shall be placed on the packaging of the individual device.
22. 4.4.For devices exclusively intended for retail point of sale the UDI-PIs in AIDC shall not be required to appear on the point of sale packaging.
23. 4.5.When AIDC carriers other than the UDI carrier are part of the product labelling, the UDI carrier shall be readily identifiable.
24. 4.6.If linear bar codes are used, the UDI-DI and UDI-PI may be concatenated or non-concatenated in two or more bar codes. All parts and elements of the linear bar code shall be distinguishable and identifiable.
25. 4.7.If there are significant constraints limiting the use of both AIDC and HRI on the label, only the AIDC format shall be required to appear on the label. For devices intended to be used outside healthcare facilities, such as devices for home care, the HRI shall however appear on the label even if this results in there being no space for the AIDC.
26. 4.8.The HRI format shall follow the rules of the UDI code-issuing entity.
27. 4.9.If the manufacturer is using RFID technology, a linear or 2D bar code in line with the standard provided by the issuing entities shall also be provided on the label.
28. 4.10.Devices that are reusable shall bear a UDI carrier on the device itself. The UDI carrier for reusable devices that require cleaning, disinfection, sterilisation or refurbishing between patient uses shall be permanent and readable after each process performed to make the device ready for the subsequent use throughout the intended lifetime of the device. The requirement of this Section shall not apply to devices in the following circumstances:
    1. any type of direct marking would interfere with the safety or performance of the device;
    2. the device cannot be directly marked because it is not technologically feasible.
29. 4.11.The UDI carrier shall be readable during normal use and throughout the intended lifetime of the device.
30. 4.12.If the UDI carrier is readily readable or, in the case of AIDC, scannable, through the device’s packaging, the placing of the UDI carrier on the packaging shall not be required.
31. 4.13.In the case of single finished devices made up of multiple parts that must be assembled before their first use, it shall be sufficient to place the UDI carrier on only one part of each device.
32. 4.14.The UDI carrier shall be placed in a manner such that the AIDC can be accessed during normal operation or storage.
33. 4.15.Bar code carriers that include both a UDI-DI and a UDI-PI may also include essential data for the device to operate or other data.
34. 5.General principles of the UDI database
35. 5.1.The UDI database shall support the use of all core UDI database data elements referred to in Part B of this Annex.
36. 5.2.Manufacturers shall be responsible for the initial submission and updates of the identifying information and other device data elements in the UDI database.
37. 5.3.Appropriate methods/procedures for validation of the data provided shall be implemented.
38. 5.4.Manufacturers shall periodically verify the correctness of all of the data relevant to devices they have placed on the market, except for devices that are no longer available on the market.
39. 5.5.The presence of the device UDI-DI in the UDI database shall not be assumed to mean that the device is in conformity with this Regulation.
40. 5.6.The database shall allow for the linking of all the packaging levels of the device.
41. 5.7.The data for new UDI-DIs shall be available at the time the device is placed on the market.
42. 5.8.Manufacturers shall update the relevant UDI database record within 30 days of a change being made to an element, which does not require a new UDI-DI.
43. 5.9.Internationally-accepted standards for data submission and updates shall, wherever possible, be used by the UDI database.
44. 5.10.The user interface of the UDI database shall be available in all official languages of the Union. The use of free-text fields shall, however, be minimized in order to reduce translations.
45. 5.11.Data relating to devices that are no longer available on the market shall be retained in the UDI database.
46. 6.Rules for specific device types
47. 6.1.Implantable devices:
48. 6.1.1.Implantable devices shall, at their lowest level of packaging (‘unit packs’), be identified, or marked using AIDC, with a UDI (UDI-DI + UDI-PI);
49. 6.1.2.The UDI-PI shall have at least the following characteristics:
    1. the serial number for active implantable devices,
    2. the serial number or lot number for other implantable devices.
50. 6.1.3.The UDI of the implantable device shall be identifiable prior to implantation.
51. 6.2.Reusable devices requiring cleaning, disinfection, sterilisation or refurbishing between uses
52. 6.2.1.The UDI of such devices shall be placed on the device and be readable after each procedure to make the device ready for the next use.
53. 6.2.2.The UDI-PI characteristics such as the lot or serial number shall be defined by the manufacturer.
54. 6.3.Systems and procedure packs as referred to in Article 22
55. 6.3.1.The natural or legal person referred to in Article 22 shall be responsible for identifying the system or procedure pack with a UDI including both UDI-DI and UDI-PI.
56. 6.3.2.Device contents of system or procedure packs shall bear a UDI carrier on their packaging or on the device itself.

    Exemptions:

    1. individual single-use disposable devices, the uses of which are generally known to the persons by whom they are intended to be used, which are contained within a system or procedure pack, and which are not intended for individual use outside the context of the system or procedure pack, shall not be required to bear their own UDI carrier;
    2. devices that are exempted from bearing a UDI carrier on the relevant level of packaging shall not be required to bear a UDI carrier when included within a system or procedure pack.
57. 6.3.3.Placement of the UDI carrier on systems or procedure packs
    1. The system or procedure pack UDI carrier shall as a general rule be affixed to the outside of the packaging.
    2. The UDI carrier shall be readable, or, in the case of AIDC, scannable, whether placed on the outside of the packaging of the system or procedure pack or inside transparent packaging.
58. 6.4.Configurable devices:
59. 6.4.1.A UDI shall be assigned to the configurable device in its entirety and shall be called the configurable device UDI.
60. 6.4.2.The configurable device UDI-DI shall be assigned to groups of configurations, not per configuration within the group. A group of configurations is defined as the collection of possible configurations for a given device as described in the technical documentation.
61. 6.4.3.A configurable device UDI-PI shall be assigned to each individual configurable device.
62. 6.4.4.The carrier of the configurable device UDI shall be placed on the assembly that is most unlikely to be exchanged during the lifetime of the system and shall be identified as the configurable device UDI.
63. 6.4.5.Each component that is considered a device and is commercially available on its own shall be assigned a separate UDI.
64. 6.5.Device Software
65. 6.5.1.UDI assignment Criteria

    The UDI shall be assigned at the system level of the software. Only software which is commercially available on its own and software which constitutes a device in itself shall be subject to that requirement.

    The software identification shall be considered to be the manufacturing control mechanism and shall be displayed in the UDI-PI.

66. 6.5.2.A new UDI-DI shall be required whenever there is a modification that changes:
    1. the original performance;
    2. the safety or the intended use of the software;
    3. interpretation of data.

    Such modifications include new or modified algorithms, database structures, operating platform, architecture or new user interfaces or new channels for interoperability.

67. <div class="mb"6.5.3.Minor software revisions shall require a new UDI-PI and not a new UDI-DI.