T3799 Additional trade item identification type code

T3799 Additional trade item identification type code

Code Name Description Used in Sweden
ADMDM Agence du Médicament de Madagascar Agency du Médicament de Madagascar manages the market authorisation of healthcare products in Madagascar - MG
AIG Active Ingredient Number The Active Ingredient Group Number specifies the a number assigned by Health Canada in the Drug Product Database. The AIG number is a 10 digit number that identifies products that have the same active ingredient(s) and ingredient strength(s).
ANVISA National Health Surveillance Agency (ANVISA) National Health Surveillance Agency (ANVISA) manages the market authorisation of healthcare products in Brazil - BR
ARFA Agência de Regulação e Supervisão dos Produtos Farmacêuticos e Alimentares (ARFA) Agência de Regulação e Supervisão dos Produtos Farmacêuticos e Alimentares (ARFA) manages the market authorisation of healthcare products in Cape Verde - CV
ARTG_ID Australian Register of Therapeutic Goods The Australian Therapeutic Goods Administration (TGA) is a government organisation responsible for the regulation of therapeutic goods such as medicines and medical devices. Once a product is accepted for sale in Australia (via TGA approval) this item is listed on the Australian Register of Therapeutic Goods (ARTG). All goods within Australia, or to be exported from Australia, must be present on this list before they can be available. Information held in the database includes the name of the product, what it contains and manufacturer details.
AU_PROSTHESES_REBATE_CODE Australian Prostheses Rebate Code In Australia the federal government, through the Department of Health and Ageing, provide a rebate to private health hospitals or clinics to cover the cost of any prostheses that are fitted to a patient. This rebate is designed to cover the costs incurred by the provider. Every product is given a ‘billing code’ from the Department of Health and Ageing. This is used by the provider to communicate the rebate request to the government.
BFR BFR The Federal Institute for Risk Assessment (BFR) in the field of consumer health protection. It is the scientific agency of the Federal Republic of Germany which is responsible for preparing expert reports and opinions on food and feed safety as well as on the safety of substances and products. In this context, the Institute plays an important role in improving consumer protection and food safety. BFR reports to the Federal Ministry of Food, Agriculture and Consumer Protection (BMELV). The BFR number is a so-called product identification element (PI element). The PI element consists of the five-digit BFR company code and a four-digit number allocated by the manufacturer itself. The number sequence ends with details of the hazard characteristics of the product (for instance, irritant, corrosive or toxic).
BNDA Bahamas National Drug Agency (BNDA) Bahamas National Drug Agency (BNDA) manages the market authorisation of healthcare products in Bahamas - BS
BUYER_ASSIGNED Buyer Assigned A proprietary internal identification number assigned by a data recipient, used to identify trade items purchased from each trading partner with whom they engage in a commercial relationship. X
CDSCO Central Drugs Standard Control Organization (CDSCO) Central Drugs Standard Control Organization (CDSCO) manages the market authorisation of healthcare products in India - IN
DAV Drug Administration of Vietnam (DAV) Drug Administration of Vietnam (DAV) manages the market authorisation of healthcare products in Viet Nam - VN
DDA_NP Department of Drug Administration (DDA) Department of Drug Administration (DDA) manages the market authorisation of healthcare products in Nepal - NP
DDF_KH Department of Drugs and Food (DDF) Department of Drugs and Food (DDF) manages the market authorisation of healthcare products in Cambodia - KH
DDSME Department of Drug Supply and Medical Equipment Department of Drug Supply and Medical Equipment manages the market authorisation of healthcare products in Kyrgyzstan - KG
DGDA Directorate General of Drug Administration (DGDA) Directorate General of Drug Administration (DGDA) manages the market authorisation of healthcare products in Bangladesh - BD
DGPML_BF Direction Générale de la Pharmacie, du Médicament et des Laboratoires (DGPML) Direction Générale de la Pharmacie, du Médicament et des Laboratoires (DGPML) manages the market authorisation of healthcare products in Burkina Faso - BF
DGPML_BJ Direction General of Pharmacy, Medicine and Pharmacy Laboratories (DGPML) Direction General of Pharmacy, Medicine and Pharmacy Laboratories (DGPML) manages the market authorisation of healthcare products in Benin - BJ
DGRS Direccion General de Regulacion Sanitaria (DGRS) Direccion General de Regulacion Sanitaria (DGRS) manages the market authorisation of healthcare products in Honduras - HN
DIGEMID_MINSA Dirección General de Medicamentos (DIGEMID-MINSA) Dirección General de Medicamentos (DIGEMID-MINSA) manages the market authorisation of healthcare products in Peru - PE
DIN DIN The Drug Identification Number: The number located on the label of prescription and over-the-counter drug products that have been evaluated by the Therapeutic Products Directorate (TPD) and approved for sale in Canada.
DIN_HM DIN HM Drug Identification Number – Homeopathic: This is the number located on the label of homeopathic drug products that have been approved for sale in Canada.
DISTRIBUTOR_ASSIGNED not defined The additional Trade Item Identification value populated has been developed and assigned by an entity which purchases and takes title to goods which are then resold / redistributed elsewhere. X
DLP Direction des Laboratoires et des Pharmacies Direction des Laboratoires et des Pharmacies manages the market authorisation of healthcare products in Comoros - KM
DNM_SV Dirección Nacional de Medicamentos (DNM) Dirección Nacional de Medicamentos (DNM) manages the market authorisation of healthcare products in El Salvador - SV
DNPL Direction Nationale de la Pharmacie et du Laboratoire Direction Nationale de la Pharmacie et du Laboratoire manages the market authorisation of healthcare products in Guinea - GN
DPL Direction de la Pharmacie et des Laboratoires Direction de la Pharmacie et des Laboratoires manages the market authorisation of healthcare products in Senegal - SN
DPLMT Direction des Dervices Pharmaceutiques des Laboratoires et de la Médecine Traditionnelle Direction des services Pharmaceutiques des laboratoires et de la Médecine Traditionnelle manages the market authorisation of healthcare products in Central African Republic - CF
DPML Direction de la Pharmacie, du Médicament et des Laboratoires (DPML) Direction de la Pharmacie, du Médicament et des Laboratoires (DPML) manages the market authorisation of healthcare products in Cameroon - CM
DPMLMOH Department of Pharmacy, Medicines and Laboratory, Ministry of Health Department of Pharmacy, Medicines and Laboratory, Ministry of Health manages the market authorisation of healthcare products in Burundi - BI
DPM_CD Direction de la Pharmacie et du Médicament DPM Democratic Republic of Congo Direction de la Pharmacie et du Médicament (DPM) manages the market authorisation of healthcare products in Congo, Democratic Republic of - CD
DPM_CI Direction de la Pharmacie et du Médicament DPM Côte d'Ivoire Direction de la Pharmacie et du Médicament (DPM) manages the market authorisation of healthcare products in Côte d'Ivoire - CI
DPM_ML Direction de la Pharmacie et du Médicament Direction de la Pharmacie et du Médicament manages the market authorisation of healthcare products in Mali - ML
DRAP Drug Regulatory Authority of Pakistan (DRAP) Drug Regulatory Authority of Pakistan (DRAP) manages the market authorisation of healthcare products in Pakistan - PK
DRA_BT Drug Regulatory Authority (DRA) Drug Regulatory Authority (DRA) manages the market authorisation of healthcare products in Bhutan - BT
DTAMOH Directorate of Technical Affairs in the Ministry of Health Directorate of Technical Affairs in the Ministry of Health manages the market authorisation of healthcare products in Iraq - IQ
EDA Egyptian Drug Authority (EDA) Egyptian Drug Authority (EDA) manages the market authorisation of healthcare products in Egypt - EG
EPD EPD Electronisk Produkt Database Identifier:
EU_MEDICAL_PRODUCT_NUMBER EU Medical Product Number The European Commission for Public Health has procedures for centrally authorised medical products, and holds community registers for: - medical products for human use (regulation (EC) 726/2004) - orphan medical products for human use (regulation (EC) N141/2000) - veterinary medical products (regulation (EE) 726/2004).
FDA_MEDICAL_DEVICE_LISTING FDA Medical Device Listing Most Owners or operators of places of business (also called establishments or facilities) that are involved in the production and distribution of medical devices intended for use in the United States (U.S.) are required to list the devices that are made at their facility and the activities that are performed on those devices. Registration and listing provides FDA with the location of medical device establishments and the devices manufactured at those establishments. Knowing where devices are made increases the nation’s ability to prepare for and respond to public health emergencies.
FDA_MM Food and Drug Administration (FDA) Myanmar Food and Drug Administration (FDA) manages the market authorisation of healthcare products in Myanmar - MM
FDA_NDC_10 FDA NDC 10 The National Drug Code of the United States of America is a unique 10-digit, 3-segment number assigned to each medication listed under Section 510 of the U.S. Federal Food, Drug, and Cosmetic Act. The number identifies the labeller or vendor, product, and trade package size.
FDA_NDC_11 not defined The National Drug Code of the United States of America is a unique 11-digit, 3-segment number assigned to each medication listed under Section 510 of the U.S. Federal Food, Drug, and Cosmetic Act. The number identifies the labeller or vendor, product, and trade package size.
FDA_PH Food and Drug Administration (FDA) Philippines Food and Drug Administration (FDA) manages the market authorisation of healthcare products in Philippines - PH
FDA_PRODUCT_CODE FDA Product Code The FDA Product Code describes a product or a group of products. It is a seven-character alphanumeric string composed of five components, the Product Industry Code, the Class Code, the Subclass Code, the Process Indicator Code, and the Group Code. For more in-depth information about the FDA Product Code, see Lessons 1, 3 and 4 of the FDA Office of Regulatory Affairs (ORA) Product Code Builder Tutorial (http://www.accessdata.fda.gov/scripts/ora/pcb/tutorial/tutorial.cfm).
FDA_TH Thai Food and Drug Administration (Thai FDA) Thai Food and Drug Administration (Thai FDA) manages the market authorisation of healthcare products in Thailand - TH
FDB Food and Drugs Board (FDB) Food and Drugs Board (FDB) manages the market authorisation of healthcare products in Ghana - GH
FDD Food and Drug Department Food and Drug Department manages the market authorisation of healthcare products in Lao People’s Democratic Republic - LA
FMHACA_ET Food, Medicine and Health Care Administration and Control of Ethiopia (FMHACA) Food, Medicine and Health Care Administration and Control of Ethiopia (FMHACA) manages the market authorisation of healthcare products in Ethiopia - ET
FOR_INTERNAL_USE_1 For internal use 1 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_10 For internal use 10 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_11 For internal use 11 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_12 For internal use 12 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_13 For internal use 13 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_14 For internal use 14 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_15 For internal use 15 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_16 For internal use 16 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_17 For internal use 17 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_18 For internal use 18 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_19 For internal use 19 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_2 For internal use 2 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_20 For internal use 20 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_3 For internal use 3 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_4 For internal use 4 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_5 For internal use 5 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_6 For internal use 6 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_7 For internal use 7 Identification used for internal mapping purposes.
FOR_INTERNAL_USE_8 For internal use 8 Internal identification used for mapping purposes.
FOR_INTERNAL_USE_9 For internal use 9 Internal identification used for mapping purposes.
GDPA General Directorate of Pharmaceutical Affairs (GDPA) General Directorate of Pharmaceutical Affairs (GDPA) manages the market authorisation of healthcare products in Afghanistan - AF
GTIN_12 GTIN 12 The 12-digit GS1 Identification Key composed of a U.P.C. Company Prefix, Item Reference, and Check Digit used to identify trade items.
GTIN_13 GTIN 13 The 13-digit GS1 Identification Key composed of a GS1 Company Prefix, Item Reference, and Check Digit used to identify trade items.
GTIN_14 GTIN 14 The 14-digit GS1 Identification Key composed of an Indicator digit (1-9), GS1 Company Prefix, Item Reference, and Check Digit used to identify trade items.
GTIN_8 GTIN 8 The 8-digit GS1 Identification Key composed of a GS1-8 Prefix, Item Reference, and Check Digit used to identify trade items.
HIBC HIBC Health Industry Business Communication Barcode: An alphanumeric identification number used as a common identifier within the healthcare industry across different locations. In the Netherlands, this code is managed by the European Health Industry Business Communications Council.
ICCBBA ICCBBA ICCBBA is an international non-governmental organization (NGO) that manages, develops and licenses ISBT 128; the international information standard for the terminology, coding and labelling of medical products of human origin. ICCBBA manage the allocation of globally unique identifiers to licensed facilities and maintain the ISBT 128 Standard, international databases for Facility Identification Numbers and Product Coding, supporting documentation, and educational materials.
INDUSTRY_ASSIGNED Industry Assigned A unique proprietary identification number assigned by an industry sector association or other organisation, used to identify an item or service. Typically the association or organisation provides the industry sector with an identification number as key identifier of a type of trade item.
INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos (INVIMA) Instituto Nacional de Vigilancia de Medicamentos y Alimentos (INVIMA) manages the market authorisation of healthcare products in Colombia - CO
INVIMA INVIMA National Institute of Surveillance of Medications and Foods for Colombia. This organisation has developed a unique code of medications (CUM).
ISBN_NUMBER ISBN number International Standard Book Number: A unique numeric commercial book identifier.
ISSN_NUMBER ISSN number International Standard Serial Number: unique eight-digit number used to identify a print or electronic periodical publication.
JFDA Jordan Food and Drug Administration Jordan Food and Drug Administration manages the market authorisation of healthcare products in Jordan - JO
LMHPRA Liberia Medicines and Health Products Regulatory Authority Liberia Medicines and Health Products Regulatory Authority manages the market authorisation of healthcare products in Liberia - LR
LOTTERY_GAME_NUMBER Lottery Game Number Unknown
LOTTERY_PACK_BOOK_NUMBER Lottery pack book number A unique identifier for a book of shrink-wrapped lottery game tickets.
MANUFACTURER_PART_NUMBER Manufacturer part number The additional Trade Item Identification value populated is an identifier of a part used for an item. While the name implies that the number is assigned by the manufacturer, the part may be built by one manufacturer to apply to another manufacturer’s item. In this case this number is the applicable part number from the item’s manufacturer. The part manufacturer numbers would be found with the type of MODEL_NUMBER, SUPPLIER_ASSIGNED, or DISTRIBUTOR_ASSIGNED. For example, a 1957 car manufactured by Chevrolet has a part number AB123 which is the driver’s door handle. A secondary manufacture produces an equivalent or Original Equipment Manufacturer (OEM) part with their number of 57-123CHEV. This value would be the AB123 to signify that it is that equivalent.
MCAZ Medicines Control Authority of Zimbabwe (MCAZ) Medicines Control Authority of Zimbabwe (MCAZ) manages the market authorisation of healthcare products in Zimbabwe - ZW
MCC Medicines Control Council (MCC) Medicines Control Council (MCC) manages the market authorisation of healthcare products in South Africa - ZA
MDL MDL The Canadian Medical Device License (MDL) is required for companies which sell Class II, III, and IV medical devices in Canada. The MDL is a product approval and should not be confused with the MDEL which is a permit for the company/distributor itself.
MINSA Ministerio de Salud - Direccion de Farmacias (MINSA) Ministerio de Salud - Direccion de Farmacias (MINSA) manages the market authorisation of healthcare products in Nicaragua - NI
MISAU Departamento Farmacêutico-MISAU Departamento Farmacêutico-MISAU manages the market authorisation of healthcare products in Mozambique - MZ
MODEL_NUMBER Model Number The additional Trade Item Identification value populated is an identification number which defines the configuration of the product in addition to the Item number. This is typically printed or otherwise attached to an item. In electronics, this number is typically found around or near a serial number
MOHSW Ministry of Health & Social Welfare Ministry of Health & Social Welfare manages the market authorisation of healthcare products in Gambia - GM
MOH_AO Ministry of Health (MOH) Angola Ministry of Health (MOH) manages the market authorisation of healthcare products in Angola - AO
MOH_BB Ministry of Health (MOH) Barbados Ministry of Health (MOH) manages the market authorisation of healthcare products in Barbados - BB
MOH_BW Drugs Regulatory Unit (DRU) of the Ministry of Health (MOH) Drugs Regulatory Unit (DRU) of the Ministry of Health (MOH) manages the market authorisation of healthcare products in Botswana - BW
MOH_GY Ministry of Health - Guyana Ministry of Health manages the market authorisation of healthcare products in Guyana - GY
MOH_MA Ministry of Health - Morocco Ministry of Health manages the market authorisation of healthcare products in Morocco - MA
MOH_MR Ministry of Health: Pharmacy and Laboratory Ministry of Health: Pharmacy and Laboratory manages the market authorisation of healthcare products in Mauritania - MR
MOH_RW Ministry of Health - Rwanda Ministry of Health manages the market authorisation of healthcare products in Rwanda - RW
MOH_SZ Ministry of Health (MOH) Swaziland Ministry of Health (MOH) manages the market authorisation of healthcare products in Swaziland - SZ
MOH_TJ Ministry of Health - Tajikistan Ministry of Health manages the market authorisation of healthcare products in Tajikistan - TJ
MOH_TT Chemistry Food and Drugs Division/Ministry of Health (CFFD/MOH) Chemistry Food and Drugs Division/Ministry of Health (CFFD/MOH) manages the market authorisation of healthcare products in Trinidad and Tobago - TT
MOH_UG National Drug Authority National Drug Authority manages the market authorisation of healthcare products in Uganda - UG
MOH_UZ Ministry of Health - Uzbekistan Ministry of Health manages the market authorisation of healthcare products in Uzbekistan - UZ
MOPH_NE Ministry of Public Health Ministry of Public Health manages the market authorisation of healthcare products in Niger - NE
MOPH_TD Minister of Public Health: Direction de la Pharmacie, du Médicament et des Laboratoires Minister of Public Health: Direction de la Pharmacie, du Médicament et des Laboratoires manages the market authorisation of healthcare products in Chad - TD
MRA Medicines Regulatory Authority (MRA) Palestine Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in Palestine, State of - PS
MRA_PG Medicines Regulatory Authority (MRA) Papua New Guinea Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in Papua New Guinea - PG
MRA_SS Medicines Regulatory Authority (MRA) South Sudan Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in South Sudan - SS
MSD Unidad de Medicamentos y Tecnología en Salud (MSD) Unidad de Medicamentos y Tecnología en Salud (MSD) manages the market authorisation of healthcare products in Bolivia - BO
MSP Direccion General de Drogas y Farmacias del Ministerio de Salud Pública (DGDF/MSP) Direccion General de Drogas y Farmacias del Ministerio de Salud Pública (DGDF/MSP) manages the market authorisation of healthcare products in Dominican Republic - DO
MSPAS_CG Ministère de la Santé Publique et des Affairs Sociales: Direction des Pharmacies, du Médicament et des Laboratoires Ministère de la Santé Publique et des Affairs Sociales: Direction des Pharmacies, du Médicament et des Laboratoires manages the market authorisation of healthcare products in Congo, Republic of - CG
MSPAS_GT Minsiterio de Salud Publica y Asistencia Social/Departamento de Regulación y Control de Productos Farmacéuticos y Afines (MSPAS) Minsiterio de Salud Publica y Asistencia Social/Departamento de Regulación y Control de Productos Farmacéuticos y Afines (MSPAS) manages the market authorisation of healthcare products in Guatemala - GT
MSPBS Ministerio de Salud Pública y Bienestar Social (MSPBS) Ministerio de Salud Pública y Bienestar Social (MSPBS) manages the market authorisation of healthcare products in Paraguay - PY
NABCA_PRODUCT_CODE NABCA product code A product code issued by the National Alcohol Beverage Control Association in the United States.
NADFC National Agency of Drug and Food Control (NADFC) National Agency of Drug and Food Control (NADFC) manages the market authorisation of healthcare products in Indonesia - ID
NAFDAC_NG National Agency for Food and Drug Administration and Control (NAFDAC) National Agency for Food and Drug Administration and Control (NAFDAC) manages the market authorisation of healthcare products in Nigeria - NG
NAN Nordic Item Number Nordic Article Number is a 6 digit identification number needed on all human and veterinary pharmaceuticals licensed in Sweden. The number is unique for a certain packages. A NAN can be valid in one to five Nordic countries (Sweden, Denmark, Norway, Finland and Iceland) depending on if the package fulfils some basic criteria. X
NCM National Center for Medicines, Medical Devices and Medical Equipment Expertise National Center for medicines, medical devices and medical equipment expertise manages the market authorisation of healthcare products in Kazakhstan - KZ
NMFA National Medicines and Food Administration National Medicines and Food Administration manages the market authorisation of healthcare products in Eritrea - ER
NMPB_SD National Medicines and Poisons Board (NMPB) National Medicines and Poisons Board (NMPB) manages the market authorisation of healthcare products in Sudan - SD
NMRA_LK National Medicines Regulatory Authority (NMRA) National Medicines Regulatory Authority (NMRA) manages the market authorisation of healthcare products in Sri Lanka - LK
NMRC Namibia Medicines Regulatory Council Namibia Medicines Regulatory Council manages the market authorisation of healthcare products in Namibia - NA
NPN NPN The Natural Health Product Number: Identifies the trade item as a natural health product and the number is assigned by a regulatory health organization for example the Health Canada - Natural Health Products Directorate (Health Canada).
NSN NSN UN/ECE Rec 24 - Fully Adopted by GS1
NUMERO_RDN RDN An identification number assigned by the Italian Ministry of Health to medical devices treated by the national health system
NZ_MEDICINES_TERMINOLOGY_CODE NZ Medicines Terminology Code For medicines used within NZ healthcare, the code assigned by NZULM (New Zealand List of Medicines). The NZ Medicines Terminology Code on the NZULM website is referred to as the SCTID (Snomed Concept ID).
PBSL Pharmacy Board of Sierra Leone Pharmacy Board of Sierra Leone manages the market authorisation of healthcare products in Sierra Leone - SL
PCOJ Pharmacy Council of Jamaica (PCoJ) Pharmacy Council of Jamaica (PCoJ) manages the market authorisation of healthcare products in Jamaica - JM
PHARMACODE_CH Pharmacode CH A national drug code for Switzerland assigned by e-mediat AG, Bern. The identification number based on the standard Code39 and is used in the whole Swiss healthcare market.
PIRC Pharmaceutical Inspectorate and the Registration Committee Pharmaceutical Inspectorate and the Registration Committee manages the market authorisation of healthcare products in Suriname - SR
PLU PLU-number A number used to indicate a price look up for an existing random weight item. This is only used for items that have been assigned an industry PLU or proprietary PLU and that are utilized through a weighing system through the scales at the back or the front registers. X
PMPB Pharmacy, Medicines and Poisons Board Pharmacy, Medicines and Poisons Board manages the market authorisation of healthcare products in Malawi - MW
PPB Pharmacy and Poisons Board Pharmacy and Poisons Board manages the market authorisation of healthcare products in Kenya - KE
RVG RVG (Register Verpakte Geneesmiddelen): An identification number provided by the Institute for Drug Evaluation (College ter Beoordeling van Geneesmiddelen – CBG) in the Netherlands. This number is used as the main identification for all drugs that have been approved by the CBG for distribution within the Netherlands.
RVH RVH (Register Verpakte Homeopatische Geneesmiddelen): An identification number provided by the Institute for Drug Evaluation (College ter Beoordeling van Geneesmiddelen – CBG) in the Netherlands. This number is used as the main identification for all homeopathic drugs that have been approved by the CBG for distribution within the Netherlands.
SAN_4 SAN 4 A nationally set standard trade item number for a variable measure trade item. The SAN-4 is a four-digit number that uniquely identifies a weight trade item according to its country of origin. This short number is incorporated into the 13 digit GTIN symbol in combination with the weight, quantity or price.
SBDMA Supreme Board for Drugs & Medical Appliances Supreme Board for Drugs & Medical Appliances manages the market authorisation of healthcare products in Yemen - YE
SCDMTE The Scientific Centre of Drug and Medical Technologies Expertise (SCDMTE) The Scientific Center of Drug and Medical Technologies Expertise (SCDMTE) manages the market authorisation of healthcare products in Armenia - AM
SFDA State Food Drug Administration (SFDA) State Food Drug Administration (SFDA) manages the market authorisation of healthcare products in China - CN
SMDC_UA State Service of Ukraine on Medicines and Drugs Control (SMDC) State Service of Ukraine on Medicines and Drugs Control (SMDC) manages the market authorisation of healthcare products in Ukraine - UA
SRAMA State Regulatory Agency for Medical Activities State Regulatory Agency for Medical Activities manages the market authorisation of healthcare products in Georgia - GE
SUPPLIER_ASSIGNED Supplier Assigned The additional Trade Item Identification value populated has been developed and assigned by the party which provides service(s) and/or manufactures or otherwise has possession the goods and consigns or makes them available in trade. Note! The value SUPPLIER_ASSIGNED should not be selected at term T3799. Supplier's article number is selected at T0172. X
TFDA Tanzania Food and Drugs Authority (TFDA) Tanzania Food and Drugs Authority (TFDA) manages the market authorisation of healthcare products in Tanzania - TZ
WAND_NUMBER WAND Number The identification code assigned from the WAND (Web Assisted Notification of Devices) database.
ZAMRA Zambia Medicines Regulatory Authority (ZAMRA) Zambia Medicines Regulatory Authority (ZAMRA) manages the market authorisation of healthcare products in Zambia - ZM
Z_INDEX Z INDEX An additional identification number used to identify all medical supplies and drugs in the Netherlands when managing reimbursements for the items. The Z-Index number is assigned to every product by Z-Index, which is a regulatory body in the Netherlands for the healthcare industry.