T4238 Additional trade item classification system code

Code value Name Description Used in Sweden
1 GXS GXS Product Data Quality (Formerly UDEX LTD)
2 IRI IRI
3 AC Nielsen AC Nielsen
4 GS1 Canada ECCnet A product classification system ECCnet Classification Codes maintained by GS1 Canada and used by the GS1 Canada ECCnet Registry.
5 UNSPSC United Nations Standard Products and Services Code
6 ECCMA ECCMA - Electronic Commerce Code Management Association
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
8 Supplier Assigned A manufacturer's own codification system
9 AMECE AMECE - Code system used in the GS1 Mexico market
10 CCG CCG - Code system used in the GS1 Germany market
11 EANFIN EANFIN - Code system used in the GS1 Finland market
12 CFIA (Canadian Food Inspection Agency) fish list Canadian Food Inspection Agency (CFIA) fish list - The Canadian Food Inspection Agency is a regulatory agency that is dedicated to the safeguarding of food, plants, and animals in Canada.
13 IFLS5 IFLS5 - Code system used in the GS1 France market
14 CBL CBL - Code system used in the GS1 Netherlands market
15 JICFS Catalogue Item Information Service of Japan JICFS. Classification system maintained by GS1 Japan and used mainly on the Japanese market.
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 (more than 3,5 percent fat) 2 Category II - standard milk (3,0 - 3,5 percent fat) 5 Category V - medium fat milk (1,5 - 1,8 percent fat) 7 Category VII - low fat milk (less than 0,5 percent fat) 9 Category IX - other
17 GS1 Spain GS1 Spain. A product classification system maintained by GS1 Spain and used in the Spanish Market.
18 GS1 Poland GS1 Poland. A product classification system maintained by GS1 Poland.
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.
20 ECR Efficient Consumer Response (ECR) Austria
21 GS1 Italy GS1 Italy
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).
23 IFDA International Foodservice Distributors Association (IFDA)
24 AHFS American Hospital Formulary Service AHFS Pharmacologic - Therapeutic Classification (C)(AHFS)
25 ATC Anatomical Therapeutic Chemical classification (ATC)
26 ClaDiMed Classification des Dispositifs Médicaux (ClaDiMed)
27 CMDR Canadian Medical Device Regulations (CMDR)
28 CND Classificazione Nazionale dei Dispositivi Medici (CND)
30 UKDM and D UK Dictionary of Medicines and Devices( DM and D) Standard Coding Scheme
31 eCl@ss Standardized Material and Service Classification and Dictionary
32 EDMA Standardized Material and Service Classification and Dictionary
33 EGAR European Generic Article Register Classification (EGAR ) standard for medical devices
34 IMS European Generic Article Register Classification (EGAR ) standard for medical devices
35 GMDN Global Medical Devices Nomenclature (GMDN)
36 GPI Generic Product Identifier (GPI). A drug code list managed by Medi-Span.
37 HCPCS Healthcare Common Procedure Coding System (HCPCS): Pronounced as Hick Picks.
38 ICPS International Classification for Patient Safety (ICPS). For use in Field Testing in 2007-2008 (WHO).
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).
40 Medical Columbus German Medical classification system.
41 NAPCS North American Classification System (NAPCS)
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.
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.
44 SHPA The Society of Hospital Pharmacists of Australia (SHPA)
45 SNOMED CT Systematized Nomenclature of Medicine-Clinical Terms ( SNOMED CT (R) )
46 UMDNS Universal Medical Device Nomenclature System (UMDNS)
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.
48 FEDAS FEDAS (sport) FEDAS represents the trans-border interests of specialist sports retailers forming part of associations in European countries. It provides services for members and third parties and is a dialogue partner for all questions concerning specialist sports retailing in Europe. FEDAS has developed a uniform and unique six digit Product Classification Key for the sports retail industry (retailers, suppliers and service providers). Further more detailed information can be found under www.fedas.com.
49 EAS EAS (footwear) European Article System: A harmonised system to classify and process the characteristics of shoes across Europe.
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).
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.
52 Australian Pharmaceutical Benefits Scheme 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).
53 Australian TGA Risk Classification The Pharmaceutical Benefits Schedule lists all drugs available under the scheme and the conditions under which it may be used.
54 MIV-C The PBS is a way of the Australian government subsidising the cost of particular medicines to make them more affordable for the community.
55 MIV-D 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.
56 BTE The Repatriation Pharmaceutical Benefits Scheme is effectively the same scheme, however, offered to eligible war veterans, war widows and their dependents.
57 REV Australian TGA Risk Classification: The Therapeutic Goods Administration (TGA) have their own classification system for medical devices within Healthcare.
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).
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/.
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/
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/
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/
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
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.
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.
66 Medsafe Risk Classification Medsafe Risk Classification. The New Zealand Medical Devices Safety Authority
67 Medsafe Regulatory Classification Medsafe Regulatory Classification. The New Zealand Medicines Safety Authority
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.
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.
70 VBN Vereiniging van Bloemenveilingen in Nederland, Dutch Flower Auction Association. http://www.vbn.nl/en-US/Pages/default.aspx.
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.
72 European Community School Milk Program defined by the European Community to ensure milk products consumption at school.
73 OKPD2 Russian Classification of Product by Economic Activities. OKPD2 Russian Classification of Product by Economic Activities.
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.
75 Product Classification System for Alcohol Beverages Product Classification System for Alcohol Beverages managed by GS1 Sweden. X
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.
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.
78 Swissmedic dispensing category Swissmedic classifies medicinal products into different dispensing categories of supply. E.g., A: Single dispensing requiring a medical or veterinary prescription, B: Dispensing requiring a medical or veterinary prescription, D: Supply on the advice of a specialist, E: Supply in the absence of advice of a specialist.
79 DE_Hilfsmittelnummer The "Hilfsmittelnummer" (aid number) indicates an aid whose medical benefit has been proven. The number is assigned by the central associations of the health insurances and is, in most cases, necessary for a reimbursement by the sponsors. Medical devices will only receive an "Hilfsmittelnummer" (aid number) if their viability, safety, indication-related requirements and medical benefit have been proven by the manufacturer. In the aid directory of the statutory health insurance funds all aids with aid number are divided into categories and product groups and collected.
80 feature Valvira (Finnish National Supervisory Authority for Welfare and Health) classification of packaging for alcoholic products. https://www.valvira.fi/en/web/en/valvira Finnish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje.pdf/658d1652-e648-4ecf-86bc-07b6b3a9a699 Swedish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje_sve.pdf/b11e69cd-0f97-4ad4-af4a-76c2cd87b8a4
81 Code value not available in code list. Valvira (Finnish National Supervisory Authority for Welfare and Health) classification for alcoholic products. https://www.valvira.fi/en/web/en/valvira Finnish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje.pdf/658d1652-e648-4ecf-86bc-07b6b3a9a699 Swedish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje_sve.pdf/b11e69cd-0f97-4ad4-af4a-76c2cd87b8a4
82 Valvira Quality Class Code for wines Valvira (Finnish National Supervisory Authority for Welfare and Health) classification for wines. https://www.valvira.fi/en/web/en/valvira Finnish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje.pdf/658d1652-e648-4ecf-86bc-07b6b3a9a699 Swedish: https://www.valvira.fi/documents/14444/0/tuoterekisteriohje_sve.pdf/b11e69cd-0f97-4ad4-af4a-76c2cd87b8a4
83 BNN Classification Key of the German "Bundesverband Naturkost Naturwaren (BNN)"
84 CEST Brazilian Specification Code for Tax Substitution (CEST)
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.
86 National Healthcare Security Administration (NHSA) China National Healthcare Security Administration.
87 National Medical Products Administration (NMPA) China National Medical Products Administration.
88 European Medical Device Nomenclature (EMDN) European Medical Device Nomenclature (EMDN)
89 COFEPRIS Mexican Federal Commission for the protection Against Sanitary Risks (COFEPRIS, Comisión Federal para la Protección contra Riesgos Sanitarios) classification.
90 Czech State Veterinary Administration Classification system of animal products defined by the State Veterinary Administration (SVA) of the Czech Republic.
99 United Kingdom (UK) High in Fat Salt and Sugar (HFSS) United Kingdom (UK) High in Fat Salt and Sugar (HFSS) category code.
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