Home GUDID 10722355002900 hema-screen SPECIFIC GOLD
Primary DI 10722355002900
Brand hema-screen SPECIFIC GOLD
Company Immunostics Company, Inc
Model HSGDCAS-25
Catalog number HSGDCAS-25
Device description The hema-screen Specific Gold is for the rapid and qualitative determination of Human Blood fecal samples. It is intended for professional and laboratory use only. It is also useful for determining gastrointestinal bleeding due to a number of gastrointestinal (GI) disorders such as diverticulitis, colitis, polyps and colorectal cancer. This test is recommended for use in routine physical examines, hospital monitoring of bleeding in patients, and for screening for colorectal cancer or gastrointestinal (GI) bleeding from any source.
Published 2025-04-16
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name KHE Reagent, Occult Blood
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KHE Reagent, Occult Blood Hematology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10722355002900 Primary GS1 0 80722355002909 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10722355002900 10722355002900 80722355002909 80722355002909
GMDN Terms# Term, Definition table Term Definition Faecal occult blood IVD, kit, rapid ICT, clinical A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative screening of stool (faeces) for occult blood (haemoglobin and/or transferrin) within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 4 Degrees Celsius 30 Degrees Celsius
Regulatory Flags# DUNS number 119214195 Device count 25 Kit true Lot or batch true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00816862028324 WELLlife™ WONDFO USA CO., LTD. KHE 2026-05-15 00816917027821 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2026-03-25 10673486013993 Teco Diagnostics Rapid Fecal Occult Blood (FOB) Test TECO DIAGNOSTICS KHE 2026-01-30 10722066011338 Rapid Response BTNX Inc KHE 2026-01-02 20722066011335 Rapid Response BTNX Inc KHE 2026-01-02 00816917027173 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2025-05-02 10722355002894 hema-screen SPECIFIC GOLD Immunostics Company, Inc KHE 2025-04-16 10722355003068 hema-screen SPECIFIC GOLD Immunostics Company, Inc KHE 2025-04-16 00850036464662 Red Tunica Rodimedi & Associates, Inc. KHE 2025-03-14 20850036464666 Red Tunica Rodimedi & Associates, Inc. KHE 2025-03-14 00816862025972 WELLlife™ WONDFO USA CO., LTD. KHE 2024-12-24 10816862025979 WELLlife™ WONDFO USA CO., LTD. KHE 2024-12-24 00816917026374 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2024-06-28 00850054026590 QMedix™ Diagnostic Automation, Inc. KHE 2024-05-10 10023513132157 Reese's ColoTest REESE PHARMACEUTICAL COMPANY KHE 2024-04-26 00816917026244 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2024-02-19 10023513132140 Reese's ColoTest REESE PHARMACEUTICAL COMPANY KHE 2024-01-23 00816917026121 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2023-10-26 00810143620023 GenaCheck Rapid Self-Test Kit for FOB Genabio Diagnostics Inc. KHE 2023-10-06 10722066007102 Rapid Response BTNX Inc KHE 2023-06-15 00722066004302 Rapid Response BTNX Inc KHE 2023-06-15 00816917026015 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2023-03-14 00816917025728 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2022-04-18 00816917025704 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2022-04-08 00816917025681 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2022-03-28 00816917025582 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2021-12-20 30080196165142 Medline MEDLINE INDUSTRIES, INC. KHE 2021-10-29 10080196165148 Medline MEDLINE INDUSTRIES, INC. KHE 2021-10-29 00816917025506 OC-Light S POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC KHE 2021-10-14 B224SB191 TRI-SLIDE PATIENT ENVELOPE KIT CENOGENICS CORPORATION KHE 2021-05-27