List of Attributes
The table below provides a complete list of attributes and descriptions that are available with GHX Data Connect.
| Attribute | Description | Example | Integration |
|---|---|---|---|
| Source Type | Provider source of the data. | IM, POH, CTR, IM/POH, IM/POH/CTR, IM/CTR, POH/CTR | |
| Buyer Part # | ERP Item Identifier of part number searched. | (alpha-numeric) | |
| Provider Item Status | Status from the PCAT/IM of the provider item; Active/Inactive. | A/I | |
| Vendor (Supplier) Name | Validated Supplier Name. | Abbott Nutrition | |
| Vendor (Supplier) Part # | Validated Supplier Part #. | 55253 | X |
| Vendor Item Status | Supplier item status. | Available/Not Distributed | |
| Manufacturer Name | Validated Manufacturer Name. | Abbott Nutrition | |
| Manufacturer Part # | Validated Manufacturer Part #. | 55253 | X |
|
Manufacturer Description |
Manufacturer provided description (not always populated); no GHX standardization applied. |
ELECARE JR UNFL 14.1OZ PWD 6CT |
|
| Manufacturer Discontinued Date | Manufacturer provided; mainly from FDA's AccessGUDID. | (date format) | |
|
Manufacturer Item Status |
Manufacturer's item status. |
Active/Discontinued |
|
| Manufacturer Brand Name | Validated Manufacturer's brand name describing the product. | Kleenex | |
|
GHX UOM 1-5 |
Supplier UOM; up to 5. |
EA/BX/CA |
|
| GHX QOE 1-5 | Quantity of each related to Supplier UOM; up to 5. | 1/10/100 | |
|
Validated and enhanced GHX description. |
FORMULA amino acid medium-chain triglyceride SUPPLEMENTAL can powder Pediatric 30 cal/oz 14.1 oz malabsorption maldigestion short bowel syndrome eosinophilic gi disorder |
|
|
| GHX Noun | Validated noun describing the product. | FORMULA | |
|
GHX Type |
Validated type describing the product. |
SUPPLEMENTAL |
|
| Primary Description | Generated description per configuration in the Data Connect Content Workbench. | Battery Rechargeable Kit Manual Filterline Npb-70 Handheld | X |
|
Secondary Description |
Generated description per configuration in the Data Connect Content Workbench. |
Battery Rechargeable Kit Manual Filterline Npb-70 Handheld Capnography |
X |
| Tertiary Description | Generated description per configuration in the Data Connect Content Workbench. | Battery Rechargeable Kit Manual Filterline Npb-70 Handheld Capnography | X |
|
Quaternary Description |
Generated description per configuration in the Data Connect Content Workbench. |
Battery Rechargeable Kit Manual Filterline Npb-70 Handheld |
|
| Quinary Description | Generated description per configuration in the Data Connect Content Workbench. | Battery Rechargeable Kit Manual Filterline Npb-70 Handheld Capnography | |
|
UNSPSC Version |
United Nations Standard Products and Services Code (UNSPSC) version per configuration in the Data Connect Content Workbench. |
250901 |
|
| UNSPSC Code | UNSPSC commodity code for category. | 42231804 | X |
|
UNSPSC Commodity |
Commodity category description. |
Pediatric disease specific supplemental formulas or bars or puddings |
|
| UNSPSC Class | Class category description. | Formulas and products for nutritional support | |
|
UNSPSC Family |
Family category description. |
Clinical nutrition |
|
| UNSPSC Segment | Segment category description. | Medical Equipment and Accessories and Supplies | |
|
Lumere Product Name |
A single product or product line that shares common key FDA-related product facts, peer-reviewed literature, or adverse event information. |
Masters HP Series Mitral Valve |
|
| Lumere Product Group | A collection of functionally similar products that are used to achieve the same clinical or functional outcome. | Mechanical prosthetic mitral valves | |
|
Lumere Category |
A collection of device groups that fall under the same clinical umbrellas and are typically source together. |
Valve replacement and repair |
|
| HCPCS Code | Healthcare Common Procedure Coding System (HCPCS) code defined by CMS; assigned by GHX. | C1876 | X |
|
Status describing if product is coded, non-billable, or no code assigned by GHX. |
Coded/No Code/Non Billable |
|
|
| HCPCS Description | HCPCS code description defined by CMS. | Stent, noncoated/noncovered, with delivery system | |
|
Revenue codes are typically based on the Healthcare Common Procedure Coding System (HCPCS) Level II codes, which are alphanumeric codes used for reporting supplies, services, and equipment; assigned by GHX. |
0278 |
X |
|
| Primary Issuing Agency | The source of the device identifier. | GS1/HBICC | |
|
Primary Device Identifier (GTIN or HIBCC); An identifier that is the primary lookup for a medical device. The primary DI will be located on the label of the base package (the lowest package level if a medical device containing a full UDI). For medical devices without packaging, the primary DI number and full UDI may be on the device itself. Not always populated. |
8717648175633 |
X |
|
| Primary DI UOM | GHX uses relevant sources to assign a UOM for Primary DI. This is not provided by GUDID. | EA/BX/CA | |
|
Primary Device Count |
Number of medical devices in the base package (the lowest package level of a medical device containing a full UDI). |
10 |
|
| Unit of Use DI | Unit of Use Device Identifier Number. Does not appear on device label. Can be used by hospital staff and materials management to associate the use of a single device with a patient when the UDI is found on a higher level of packaging (e.g, on a box of 100 blood collection tubes). Not always populated. | 8717648175632 | X |
|
GHX uses relevant sources to assign a UOM for Unit of Use DI. This is not provided by GUDID. |
EA |
|
|
| Secondary Issuing Agency | The source of the device identifier. | GS1/HIBCC | |
|
The optional device identifier that may be an alternate look up for the Primary DI. A secondary DI comes from a different issuing agency than the Primary DI. Rarely populated. |
|
|
|
| Package DI (1 thru 5) | The device identifier (DI) assigned to a device package (a fixed quantity of a particular version or model of a device). Different levels of packaging have different DIs. Not always populated. | X | |
|
The Primary DI for the base package or the Package DI for any lower-level package configuration contained within a given package configuration. |
|
|
|
| Package DI UOM (1 thru 5) | Text to describe the outer packaging of the product and enables users to understand higher level packaging configurations. (Box, Case, Carton) GHX uses relevant sources to assign unit of measure. UOM in this field is only applicable when a package Device Identifier is present. | EA/BX/CA | X |
|
The number of packages with the same Primary DI or Package DI within a given packaging configuration. GHX uses relevant sources to assign quantity of each. QOE in this field is only applicable when a package Device Identifier is present. |
1/10/100 |
|
|
| Contains Latex | Validated indicator; answers the question "contains latex?" | Yes/No | X |
|
Whether the device was originally packaged to be free from viable microorganisms. Validated indicator; answers the question "is Sterile?" |
Yes/No |
X |
|
| Requires Sterilization | Whether the device requires sterilization before use on a patient. Answers the question "Requires Sterilization?" | Yes/No | |
|
Sterilization Method |
Sterilization Method(s) recommended prior to use. |
Moist heat or steam sterilization |
|
| Is Implantable | Validated indicator; answers the question "is implantable?" | Yes/No | X |
|
For Single Use |
Whether the device is intended for one use or on a single patient during a single procedure. Validated indicator; answers the question "Is for Single use?" |
Yes/No |
|
| Contains Human Tissue | Whether the product contains or consists of human cells or tissues that are intended for implantation, transplantation, infusion, or transfer into a human recipient. Pass thru information from GS1; answers the question "contains human tissue?" | Yes/No | |
|
Contains Hazardous Material |
Validated indicator; answers the question "contains hazardous material?" |
Yes/No |
|
| MRI Safety Code | What information the labeling contains about whether a device is compatible with magnetic resonance imaging (MRI) procedures. Indicates the MRI Safety Information, if any, that is present in the device labeling. | MR Unsafe/Labeling does not contain MRI Safety Information | |
|
Image URL |
URL that renders an image of the product. The image URL is not integated in the ERP systems at this time. It is available in Power Sourcing and Catalog Search. The image URL values will be in the MCAT even though they are not integrated. |
|
|
| Last Purchase Date | The last time the item was seen in the Purchase Order History. | (date format) | |
| Preferred Contract # | Matched Client Contract ID from CCX of part number searched. | (alpha-numeric) | |
| Preferred Contract UOM 1-5 | Unit of Measure for the item on contract. | ||
|
Preferred Contract QOE 1-5 |
Quantity of Each for the item on contract. |
|
|
| Preferred Contract Price | Landed contract price for the item on contract. | ||
|
Country of Origin (ESG) |
|
US |
|
| Is Reusable (ESG) | Answers the question "Is Reusable?" | Yes/No | |
| Was Reprocessed (ESG) | Answers the question "was reprocessed?" | Yes/No | |
| Duplicate Description Indicator | Duplicate descriptions for two buyer part numbers. | Yes |