T4238 Additional trade item classification system code

Code valueNameDescriptionUsed in Sweden
1GXSGXS Product Data Quality (Formerly UDEX LTD)
2IRIIRI
3AC NielsenAC Nielsen
4GS1 Canada ECCnetA product classification system ECCnet Classification Codes maintained by GS1 Canada and used by the GS1 Canada ECCnet Registry.
48FEDASFEDAS (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.
5UNSPSCUnited Nations Standard Products and Services Code
6ECCMAECCMA - Electronic Commerce Code Management Association
7EAN Norges Multibransje VaregruppestandardEAN 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
8Supplier AssignedA manufacturer's own codification system
9AMECEAMECE - Code system used in the GS1 Mexico market
10CCGCCG - Code system used in the GS1 Germany market
11EANFINEANFIN - Code system used in the GS1 Finland market
13IFLS5IFLS5 - Code system used in the GS1 France market
14CBLCBL - Code system used in the GS1 Netherlands market
15JICFSCatalogue Item Information Service of Japan JICFS. Classification system maintained by GS1 Japan and used mainly on the Japanese market.
16European UnionEuropean 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
17GS1 SpainGS1 Spain. A product classification system maintained by GS1 Spain and used in the Spanish Market.
18GS1 PolandGS1 Poland. A product classification system maintained by GS1 Poland.
19Federal 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.
20ECREfficient Consumer Response (ECR) Austria
21GS1 ItalyGS1 Italy
22CPVCommon 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).
23IFDAInternational Foodservice Distributors Association (IFDA)
24AHFSAmerican Hospital Formulary Service AHFS Pharmacologic - Therapeutic Classification (C)(AHFS)
25ATCAnatomical Therapeutic Chemical classification (ATC)
26ClaDiMedClassification des Dispositifs Médicaux (ClaDiMed)
27CMDRCanadian Medical Device Regulations (CMDR)
28CNDClassificazione Nazionale dei Dispositivi Medici (CND)
30UKDM and DUK Dictionary of Medicines and Devices( DM and D) Standard Coding Scheme
31eCl@ssStandardized Material and Service Classification and Dictionary
32EDMAStandardized Material and Service Classification and Dictionary
33EGAREuropean Generic Article Register Classification (EGAR ) standard for medical devices
34IMSEuropean Generic Article Register Classification (EGAR ) standard for medical devices
35GMDNGlobal Medical Devices Nomenclature (GMDN)
36GPIGeneric Product Identifier (GPI). A drug code list managed by Medi-Span.
37HCPCSHealthcare Common Procedure Coding System (HCPCS): Pronounced as Hick Picks.
38ICPSInternational Classification for Patient Safety (ICPS). For use in Field Testing in 2007-2008 (WHO).
39MedDRAMedical 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).
40Medical ColumbusGerman Medical classification system.
41NAPCSNorth American Classification System (NAPCS)
42NHS-eClassNational 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.
43US FDA PCCDThe 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.
44SHPAThe Society of Hospital Pharmacists of Australia (SHPA)
45SNOMED CTSystematized Nomenclature of Medicine-Clinical Terms ( SNOMED CT (R) )
46UMDNSUniversal Medical Device Nomenclature System (UMDNS)
47DTBDTB (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.
49EASEAS (footwear) European Article System: A harmonised system to classify and process the characteristics of shoes across Europe.
50Australian TGA TypeThe 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).
51Australian Medicines and Poisons Schedule CodeSUSMP: 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.
52Australian Pharmaceutical Benefits SchemeAustralian 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).
53Australian TGA Risk ClassificationThe Pharmaceutical Benefits Schedule lists all drugs available under the scheme and the conditions under which it may be used.
54MIV-CThe PBS is a way of the Australian government subsidising the cost of particular medicines to make them more affordable for the community.
55MIV-DE.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.
56BTEThe Repatriation Pharmaceutical Benefits Scheme is effectively the same scheme, however, offered to eligible war veterans, war widows and their dependents.
57REVAustralian TGA Risk Classification: The Therapeutic Goods Administration (TGA) have their own classification system for medical devices within Healthcare.
58FDA Premarket Submission NumberFDA 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).
59ETIMETIM - (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/.
60G-DRGG-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/
61ICD-GMICD-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/
62OPS-GOPS-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/
63NCMMercosur/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
64CORE DIYCORE 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.
65FDA 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.
66Medsafe Risk ClassificationMedsafe Risk Classification. The New Zealand Medical Devices Safety Authority
67Medsafe Regulatory ClassificationMedsafe Regulatory Classification. The New Zealand Medicines Safety Authority
68LPRRLPPR (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.
69INNInternational 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.
70VBNVereiniging van Bloemenveilingen in Nederland, Dutch Flower Auction Association. http://www.vbn.nl/en-US/Pages/default.aspx.
71Groupement d’Etude des Marchés en Restauration Collective et de NutritionGroupement 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.
72European Community School MilkProgram defined by the European Community to ensure milk products consumption at school.
73OKPD2 Russian Classification of Product by Economic Activities.OKPD2 Russian Classification of Product by Economic Activities.
74French Ministry of HealthThe 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.
75Product Classification System for Alcohol BeveragesProduct Classification System for Alcohol Beverages managed by GS1 Sweden.X
76EU Med Device ClassificationThe European medical device classification system is managed by the European Commission, the European Parliament and the Council of Ministers
78Swissmedic Sales CategorySwiss 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.
79DE_HilfsmittelnummerThe "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.