Home GUDID 00695684740153 COMPLIANCE GOLD iFOB PATIENT COLLECTION KITS
Primary DI 00695684740153
Brand COMPLIANCE GOLD iFOB PATIENT COLLECTION KITS
Company GERMAINE LABORATORIES, INC
Model 74015
Device description Patient collection kits for IFOB kit
Published 2016-04-27
Public version status Update
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 00695684740153 Primary GS1 0 00695684740151 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00695684740153 00695684740153 695684740153 0695684740153 00695684740151 00695684740151 695684740151 0695684740151
GMDN Terms# Term, Definition table Term Definition Faecal occult blood IVD, kit, immunochromatographic test (ICT), rapid A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative screening of stool (faeces) for occult blood (haemoglobin) within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method. This test is commonly used in the laboratory or in point-of-care analyses.
Regulatory Flags# DUNS number 176458115 Device count 15 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 10722355002900 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