Home GUDID M52550781
ColoScreen Developer 2
Primary DI M52550781
Brand ColoScreen Developer 2
Company HELENA LABORATORIES CORPORATION
Model 5078
Published 2016-08-18
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
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 M52550781 Package HIBCC 50 In Commercial Distribution M52550780 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Faecal occult blood IVD, kit, rapid colorimetric, 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) within a short period relative to standard laboratory testing procedures, using a rapid colorimetric method. This is a rapid test commonly used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.
Regulatory Flags# DUNS number 079396131 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published M5255526510 SPIFE A1AT Kit 552651 2026-06-23 M52551830 AB-Trol 3 Coagulation Control 5183 2016-08-18 M52551850 Coagulation S.A.R.P (Specialty Assayed Reference Plasma) 5185 2016-09-07 M52551860 NORM-TROL 1 Coagulation Control 5186 2016-09-07 M52551870 AB-TROL 2 Coagulation Control 5187 2016-09-07 M52553010 Coagulation S.A.C.-1 (Specialty Assay Control) 5301 2016-09-07 M52553020 Coagulation S.A.C.-2 (Specialty Assay Control) 5302 2016-09-07 M52536110 H-Pette without Blade (1000 pieces) 3611 2017-05-26 M52536120 H-Pette with Blade (1000 pieces) 3612 2017-05-26 M52536130 H-Pette Remover 3613 2017-03-17 M52536150 H-Pette II (No Blade, Metal Canula) (1000 pieces) 3615 2017-05-26 M52594230 IFE Free Lambda Light Chain Antiserum 9423 2024-09-27 M5255527370 SPIFE Nexus IFE-6 Antisera Kit 552737 2024-09-27 M5255527440 SPIFE Nexus IFE-9/15 Antisera Kit 552744 2024-09-27 M52594190 IFE IgD Antiserum 9419 2024-09-27 M52594200 IFE IgE Antiserum 9420 2024-09-27 M52594220 IFE Free Kappa Light Chain Antiserum 9422 2024-09-27 M52520050000 ProtoFluor Z (110V) 2005000 2017-03-17 M52520050020 ProtoFluor Z (110V) 2005002 2017-03-17 M52520060000 ProtoFluor Z (220V) 2006000 2017-03-17
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00810173655873 One Step Healgen Scientific Limited Liability Company KHE 2026-06-23 00810173655880 One Step Healgen Scientific Limited Liability Company KHE 2026-06-23 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