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urn:gs1:gdd:cl:AdditionalTradeItemClassificationCodeListCode
Code List : AdditionalTradeItemClassificationCodeListCode
Definition : Code list developed and managed by GS1.
Domain : Shared
Status : CURRENT
Publication Date : 23 January 2020
External Link :
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Code ValueNameDefinitionChange DateVersionStatus
1 GXS GXS Product Data Quality (Formerly UDEX LTD) 1 CURRENT
10 CCG CCG - Code system used in the GS1 Germany market 01 March 2013 2 CURRENT
11 EANFIN EANFIN - Code system used in the GS1 Finland market 01 March 2013 2 CURRENT
13 IFLS5 IFLS5 - Code system used in the GS1 France market 01 March 2013 2 CURRENT
14 CBL CBL - Code system used in the GS1 Netherlands market 01 March 2013 2 CURRENT
15 JICFS Catalogue Item Information Service of Japan JICFS. Classification system maintained by GS1 Japan and used mainly on the Japanese market. 01 March 2013 2 CURRENT
16 European Union European Union. The economic association of over a dozen European countries which seek to create a unified, barrier-free market for products and services throughout the continent. Category of product eligible for EU subsidy (applies for certain dairy products with specific level of fat content. 1 Category I - full milk (>3,5 % fat) 2 Category II - standard milk (3,0 - 3,5 % fat) 5 Category V - medium fat milk (1,5 - 1,8 % fat) 7 Category VII - low fat milk (<0,5 % fat) 9 Category IX - other 01 March 2013 2 CURRENT
17 GS1 Spain GS1 Spain. A product classification system maintained by GS1 Spain and used in the Spanish Market. 01 March 2013 2 CURRENT
18 GS1 Poland GS1 Poland. A product classification system maintained by GS1 Poland. 01 March 2013 2 CURRENT
19 Federal Agency on Technical Regulating and Metrology of the Russia Federation A Russian government agency that serves as a national standardization body of the Russian Federation. 1 CURRENT
2 IRI IRI 1 CURRENT
20 ECR Efficient Consumer Response (ECR) Austria 01 March 2013 2 CURRENT
21 GS1 Italy GS1 Italy 01 March 2013 2 CURRENT
22 CPV Common Procurement Vocabulary (CPV) was introduced in 1996 as a means of raising the level of transparency and efficiency in the field of public acquisition. The use of the standard names of the CPV facilitates the marking of the procurement contracts they are interested in. In addition, CPV facilitates the swift and exact translation of contract information for publication in the official EU Bulletin as well as the preparation of procurement statistics. The CPV code consists of eight characters as well as a control character. It is managed by the Office for Official Publications of the European Communities (OPOCE). 1 CURRENT
23 IFDA International Foodservice Distributors Association (IFDA) 1 CURRENT
24 AHFS American Hospital Formulary Service AHFS Pharmacologic - Therapeutic Classification© (AHFS) 1 CURRENT
25 ATC Anatomical Therapeutic Chemical classification (ATC) 1 CURRENT
26 ClaDiMed Classification des Dispositifs Médicaux (ClaDiMed) 1 CURRENT
27 CMDR Canadian Medical Device Regulations (CMDR) 1 CURRENT
28 CND Classificazione Nazionale dei Dispositivi Medici (CND) 1 CURRENT
3 AC Nielsen AC Nielsen 1 CURRENT
30 UKDM&D UK Dictionary of Medicines & Devices( DM&D) Standard Coding Scheme 01 March 2013 2 CURRENT
31 eCl@ss Standardized Material and Service Classification and Dictionary 1 CURRENT
32 EDMA Classification for in vitro diagnostics medical devices (EDMA) 1 CURRENT
33 EGAR European Generic Article Register Classification (EGAR ) standard for medical devices 1 CURRENT
34 IMS IMS Healthcare Generic Product Classification 1 CURRENT
35 GMDN Global Medical Devices Nomenclature (GMDN) 1 CURRENT
36 GPI Generic Product Identifier (GPI). A drug code list managed by Medi-Span. 1 CURRENT
37 HCPCS Healthcare Common Procedure Coding System (HCPCS): Pronounced as Hick Picks. 1 CURRENT
38 ICPS International Classification for Patient Safety (ICPS). For use in Field Testing in 2007-2008 (WHO). 1 CURRENT
39 MedDRA Medical Dictionary for Regulatory Activities (MedDRA): An international terminology employed by the pharmaceutical industry, medical product industry and regulatory agencies throughout the entire drug development process and product post marketing activities. The current version of MedDRA (version 10.0) contains a total of 84,906 unique terms. MedDRA terminology was developed under the auspices of the International Conference on Harmonization (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use and is a registered trademark of the International Federation of Pharmaceutical Manufacturers Associations (IFPMA). 1 CURRENT
4 GS1 Canada ECCnet A product classification system ECCnet Classification Codes maintained by GS1 Canada and used by the GS1 Canada ECCnet Registry. 10 October 2016 1 CURRENT
40 Medical Columbus German Medical classification system. 1 CURRENT
41 NAPCS North American Classification System (NAPCS) 1 CURRENT
42 NHS-eClass National Health Service (NHS) eClass: NHS-eClass is a bespoke classification system for products and services, owned by the English National Health Service (NHS). The purpose of NHS-eClass is to facilitate the accurate analysis of expenditure. 1 CURRENT
43 US FDA PCCD The Product Classification Database contains medical device names and associated information developed by the Center for Devices and Radiological Health (CDRH) in support of its mission. This database contains device names and their associated product codes. The name and product code identify the generic category of a device for FDA. The Product Code assigned to a device is based upon the medical device product classification designated under 21 CFR Parts 862-892. 01 March 2013 2 CURRENT
44 SHPA The Society of Hospital Pharmacists of Australia (SHPA) 1 CURRENT
45 SNOMED CT Systematized Nomenclature of Medicine-Clinical Terms ( SNOMED CT® ) 01 March 2013 2 CURRENT
46 UMDNS Universal Medical Device Nomenclature System (UMDNS) 01 March 2013 2 CURRENT
47 DTB DTB (fashion) Dialog Textil – Bekleiding (DTB) a German group of companies who joined forces for the TC sector. The product classification can be found on their website http://www.dialog-dtb.de if you are a member. 1 CURRENT
48 FEDAS PCK SGI-DHO (Sporting Goods Industry Data Harmonization Organization) is representing the interests of the different stakeholders of the sporting goods industry (retailers + brands). Its main task is the development and harmonisation of codes, which can be used by the sporting goods industry to exchange and analyse data. The focus is set on codes that have not already been standardised by international trade organisations. In addition to the FEDAS (the European Federation of Sporting Goods Retail Associations) product classification key that has been developed a few years ago, and which is used by may stakeholders of the sporting goods industry, SGI-DHO is working on various other codes. Under www.sgidho.com you can find further information. 1 CURRENT
49 EAS EAS (footwear) European Article System: A harmonised system to classify and process the characteristics of shoes across Europe. 1 CURRENT
5 UNSPSC United Nations Standard Products and Services Code 1 CURRENT
50 Australian TGA Type The Australian Therapeutic Goods Administration (TGA) classifies products it authorizes for sale in Australia. These items are considered either: Registered, Listed, Included or Classified as Other on the Australia Register of Therapeutic Goods (ARTG). 01 March 2013 2 CURRENT
51 Australian Medicines and Poisons Schedule Code SUSMP: An Australian classification and labelling of drugs and poisons named the Standard for the Uniform Scheduling of Medicines and Poisons (SUSMP). This was created and is maintained by the National Drugs and Poisons Scheduling Committee (NDPSC) which operates under control of the Therapeutic Goods Administration (TGA). This standard contains a list of 'Schedules', which are a way of grouping products together that may have similar regulatory controls over their availability. Criteria for scheduling may include such considerations as the purpose of use, potential for abuse, safety of use and the level of need for it. 01 March 2013 2 CURRENT
52 Australian Pharmaceutical Benefits Scheme In Australia, medicine may be subsidized by its Government via the Pharmaceutical Benefits Scheme (PBS). The PBS is a program available to all Australian residents covered under the public healthcare system (known as Medicare). The Pharmaceutical Benefits Schedule lists all drugs available under the scheme and the conditions under which it may be used. The PBS is a way of the Australian government subsidising the cost of particular medicines to make them more affordable for the community. E.g. A consumer is entitled to purchase 100 tablets of aspirin under the scheme, the retail cost is $13.00, the government subsidizes $9.50, so the consumer will pay the difference of $3.50 for the medication. The Repatriation Pharmaceutical Benefits Scheme is effectively the same scheme, however, offered to eligible war veterans, war widows and their dependents. 01 March 2013 2 CURRENT
53 Australian TGA Risk Classification The Therapeutic Goods Administration (TGA) have their own classification system for medical devices within Healthcare. The purpose of this classification is to ascertain the potential risk of a device through analysing the intended purpose of the product and using a set of classification rules. This classification allows the regulator to determine how much intervention is required before the device becomes available on the market. 01 March 2013 2 CURRENT
54 MIV-C Milch Industrie Verband Cheese Class association of the German Dairy. 01 March 2013 2 CURRENT
55 MIV-D Milch Industrie Verband Milk Class (association of the German Dairy 01 March 2013 2 CURRENT
56 BTE Bundesverband des Deutschen Textileinzelhandels a German Association of Textile Retailers. The product classification can be found on their website http://www.bte.de 01 March 2013 2 CURRENT
57 REV REV – The Office of the Revenue Commissioners: The Irish Government agency responsible for customs, excise, taxation and related matters. The division “Customs” of this office assigns classification codes to Alcohol and Tobacco for excise duties. 01 March 2013 2 CURRENT
58 FDA Premarket Submission Number FDA Premarket Submission Number is a number associated with the regulatory decision regarding the applicant’s legal right to market a medical device for the following submission types: Premarket Notification (510(k))Premarket Approval (PMA) Product Development (PDP) Humanitarian Device Exemption (HDE) Biologics License Application (BLA) New Drug Application (NDA). 20 November 2014 4 CURRENT
59 ETIM ETIM - (Europees Technisch Informatie Model or European Technical Information Model in English) is an international organisation which develops, manages and publishes one European classification for technical products. More information: http://www.etim-international.com/. 05 May 2014 3 CURRENT
6 ECCMA ECCMA - Electronic Commerce Code Management Association 01 March 2013 2 CURRENT
60 G-DRG G-DRG (German - Diagnosis Related Groups). [DRG-Entgeltkatalog] List of fees for treatment in German hospitals. Includes flat fees for entire courses of treatment (DRG) as well as additional fees for supplementary treatment components. The national associations of health insurance, the Association of Private Health Insurance and the German Hospital Federation, founded the Institute for the Hospital Remuneration System (InEK GmbH). The Institute InEK GmbH operates on behalf of the shareholders of the GmbH, the German Hospital Association, the Association of Statutory Health Insurance Funds and the Association of private health insurance. http://www.g-drg.de/cms/ 05 May 2014 3 CURRENT
61 ICD-GM ICD-GM (International Classification of Diseases – German Modification). [Diagnosen für Gesundheitsverwaltung] German modification of the International Classification of Diseases; official classification of diseases for ambulatory and stationary care in Germany. ICD was created by the World Health Organisation, and DIMDI (Deutsches Institut für Medizinische Dokumentation und Information) maintains the German modification to ICD http://www.dimdi.de/ 05 May 2014 3 CURRENT
62 OPS-G OPS-G [Operationen- und Prozedurenschlüssel] List of codes for surgical and other medical procedures, derived from the ICPM (International Classification of Procedures in Medicine), mandatory for procedure coding in hospitals and for ambulatory surgery in Germany. ICPM is maintained by the World Health Organisation, and DIMDI (Deutsches Institut für Medizinische Dokumentation und Information) maintains the German modification to it. http://www.dimdi.de/ 05 May 2014 3 CURRENT
63 NCM Mercosur/Mercosul Nomenclature (NCM): NCM is Nomenclatura Comum do MERCOSUL (MERCOSUR Common Nomenclature) Brazil, Argentina, Paraguay and Uruguay adopted the Mercosul Common Nomenclature (NCM), based on the Harmonized System Code. The eight numbers that is part of the NCM, uses the Harmonized System that forms the six first numbers, while the seventh and eighth numbers are used for specific within Mercosul. Harmonized System: The Harmonised Commodity Description and Coding System (HS) of tariff nomenclature is an internationally standardized system of names and numbers for classifying traded products developed and maintained by the World Customs Organization (WCO) (formerly the Customs Co-operation Council), an independent intergovernmental organization with over 170 member countries based in Brussels, Belgium. Example: 0104.10.11 05 May 2014 3 CURRENT
64 CORE DIY CORE DIY (Consumer Retail Classification for the Do-it-Yourself Industry) is a system for the classification of trade items with expanded product properties and specifications which provide the granularity needed for online consumer retail. CORE DIY has been developed by the do-it-yourself industry and is managed by GS1 Netherlands on behalf of the DIY user community. 05 May 2014 3 CURRENT
65 FDA Preferred Term Code, FDA Preferred Term Code, Unique four-character value assigned by the FDA to indicate a GMDN Preferred Term without exposing the GMDN PT Code. 1 CURRENT
66 Medsafe Risk Classification Medsafe Risk Classification The New Zealand Medical Devices Safety Authority 1 CURRENT
67 Medsafe Regulatory Classification Medsafe Regulatory Classification The New Zealand Medicines Safety Authority 1 CURRENT
68 LPRR LPPR (List of Products and Healthcare Services Qualifying for Reimbursement) is defined by French social security and provided for in Article L-165-1 of the Code of Social Security as a nomenclature that lists medical devices for the diagnosis, treatment diseases (e.g. diabetes) or injury (bandages), hardware support everyday life, orthotics and external prostheses, implantable devices or vehicles for the physically disabled. For each product the LPPR is applied with the refundable amount, the repayment rate and possibly its end date of repayment. 1 CURRENT
69 INN International Non-proprietary Names (INN) facilitate the identification of pharmaceutical substances or active pharmaceutical ingredients. Each INN is a unique name that is globally recognized and is public property. A non-proprietary name is also known as a generic name. 09 September 2015 4 CURRENT
7 EAN Norges Multibransje Varegruppestandard EAN Norges Multibransje Varegruppestandard - The ENVA code is used for classification and categorising of goods and it is used as an alternative to the GPC codes in the Norwegian marketplace 01 March 2013 2 CURRENT
70 VBN Vereiniging van Bloemenveilingen in Nederland, Dutch Flower Auction Association. http://www.vbn.nl/en-US/Pages/default.aspx. 08 August 2016 5 CURRENT
71 Groupement d’Etude des Marchés en Restauration Collective et de Nutrition Groupement d’Etude des Marchés en Restauration Collective et de Nutrition - French government agency that is responsible for nutritional quality of meals served in social catering. 25 January 2017 6 CURRENT
72 European Community School Milk Program defined by the European Community to ensure milk products consumption at school. 25 January 2017 6 CURRENT
73 OKPD2 Russian Classification of Product by Economic Activities. OKPD2 Russian Classification of Product by Economic Activities. 20 April 2017 7 CURRENT
74 French Ministry of Health The French Ministry of Health is the agency in charge of the code list defining the healthcare product content (and possible associated risks) for the French market. 20 April 2017 7 CURRENT
75 GS1 Sweden Alcoholic Beverages Product Classification System for Alcohol Beverages managed by GS1 Sweden. 10 February 2018 8 CURRENT
76 EU Regulation (MDR/IVDR) Risk class The Medical Devices Regulation (EU MDR 2017/745) and In-vitro-Diagnostika Regulation (EU IVDR 2017/746) risk class classification system is managed by the European Commission, the European Parliament and the Council of Ministers. 04 May 2021 9 CURRENT
77 MiGeL Position number The MiGeL item number regulates the reimbursement of medical products in the outpatient sector and is information that is required by all service providers in Switzerland in order to be able to bill service carriers. MiGel-Number applies to similar items across suppliers that have the identical number. 9 CURRENT
78 Swissmedic Sales Category Swiss Therapeutic Products Act, medicinal products authorisation procedures are divided into various supply categories. Those categories specify exactly who is permitted to supply and distribute which medicinal products, thereby ensuring competent guidance by trained specialists. Category examples are: “A” - Supply once with a prescription from a doctor or veterinarian; “B” - Supply with a prescription from a doctor or veterinarian; “C” - Supply on technical advice. 23 January 2020 10 CURRENT
8 Supplier Assigned A manufacturer's own codification system 1 CURRENT
84 CEST Brazilian Specification Code for Tax Substitution (CEST) 04 May 2021 1 CURRENT
85 EU Directive (MDD/AIMDD/IVDD) Risk class The Medical Devices Directive (MDD 93/42/EEC), Active Implantable Medical Devices Directive (90/385/EEC) and In vitro Diagnostic Medical Devices Directive (IVDD 98/79/EC) risk class classification system is managed by the European Commission, the European Parliament and the Council of Ministers. 04 May 2021 1 CURRENT
86 National Healthcare Security Administration (NHSA) China National Healthcare Security Administration. 04 May 2021 1 CURRENT
87 National Medical Products Administration (NMPA) China National Medical Products Administration. 04 May 2021 1 CURRENT
88 European Medical Device Nomenclature (EMDN) European Medical Device Nomenclature (EMDN) 04 May 2021 1 CURRENT
89 COFEPRIS Mexican Federal Commission for the protection Against Sanitary Risks (COFEPRIS, Comisión Federal para la Protección contra Riesgos Sanitarios) classification. 09 June 2021 1 CURRENT
9 AMECE AMECE - Code system used in the GS1 Mexico market 01 March 2013 2 CURRENT
SWISSMEDIC_NUMBER Swissmedic Number Every drug authorised in Switzerland is assigned such a number when it is authorised. The Swissmedic number must be printed on the package. The Swiss Medic number is a market authorization number. 23 January 2020 10 CURRENT