HEMOSURE®
- Primary DI
- 00817763020134
- Brand
- HEMOSURE®
- Company
- HEMOSURE INC.
- Model
- CM5-IUH
- Catalog number
- CM5-IUH
- Device description
- IU Health Pathology Laboratory Mailers Contains Patient Instruction and Buffer Tube; 100 Mailers/Box
- Published
- 2016-09-15
- 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
Related Records
Product Codes
| Code | Name |
|---|---|
| KHE | Reagent, Occult Blood |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| KHE | Reagent, Occult Blood | Hematology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00817763020134 | Primary | GS1 | 0 | |
| 00817763020141 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00817763020134 | 00817763020134 | 817763020134 | 0817763020134 |
| 00817763020141 | 00817763020141 | 817763020141 | 0817763020141 |
GMDN Terms
| 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. |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 2 Degrees Celsius | 30 Degrees Celsius |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 806777541
- Device count
- 100
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- 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 | Catalog | Published |
|---|---|---|---|---|
| 00817763022510 | First Sign® | FSCCUP-13124 W/AD7 | FSCCUP-13124 W/AD7 | 2024-10-16 |
| 00817763022824 | First Sign | FSCCUP-21124 | FSCCUP-21124 | 2023-07-05 |
| 00817763022367 | First Sign | FSCDIP1464 | FSCDIP1464 | 2023-05-18 |
| 00817763022572 | FIRST SIGN® | FSCDIP7364 | FSCDIP7364 | 2022-04-21 |
| 00817763022541 | First Sign® | FSCDIP7164 | FSCDIP7164P | 2020-01-08 |
| 00817763022466 | First Sign® | FSCCUP-13124 W/AD | FSCCUP-13124 W/ADP | 2019-10-21 |
| 00817763022442 | FIRST SIGN® | FSCDIP3384 | FSCDIP3384 | 2019-05-14 |
| 00817763022428 | FIRST SIGN® | FSCCUP-3864 | FSCCUP-3864 | 2019-04-29 |
| 00817763020158 | FIRST SIGN® | D0115TC-01 | D0115TC-01 | 2016-09-21 |
| 00817763020165 | FIRST SIGN® | D0115TC-02 | D0115TC-02 | 2016-09-21 |
| 00857338006163 | HEMOSURE® | T1-TC02 | T1-TC02 | 2016-08-24 |
| 00817763022244 | First Sign® | FSCCUP-6664 W/AD7 | 2018-07-23 | |
| 00817763022268 | First Sign® | FSCCUP-20104 W/AD7 | 2018-07-23 | |
| 00817763022220 | First Sign® | FSCCUP-13124 W/AD8 | 2018-06-18 | |
| 00817763022206 | First Sign® | FSCDIP1724 | 2018-05-22 | |
| 00817763022183 | First Sign® | FSCDIP5054 | 2018-05-14 | |
| 00817763022046 | First Sign® | FSCDIPBA-25 | 2018-05-09 | |
| 00817763022060 | First Sign® | FSCDIPED-25 | 2018-05-09 | |
| 00817763022084 | First Sign® | FSCDIPMD-25 | 2018-05-09 | |
| 00817763022107 | First Sign® | FSCDIPMO-25 | 2018-05-09 |
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| 10816862025979 | WELLlife™ | WONDFO USA CO., LTD. | KHE | 2024-12-24 |
| 00816917026374 | OC-Light S | POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC | KHE | 2024-06-28 |
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| 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 |
| 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 |
| 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 |
| B224SB201 | TRI-SLIDE STOOL BLOOD TEST | CENOGENICS CORPORATION | KHE | 2021-05-27 |
| B224SB211 | PROFESSIONAL SINGLE SLIDE KIT | CENOGENICS CORPORATION | KHE | 2021-05-27 |
| 00816917025223 | OC-Light S | POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC | KHE | 2020-10-26 |
| 00083059010015 | EZ Detect Fecal Occult Blood Test | BIOMERICA, INC. | KHE | 2020-07-01 |
| 00083059100013 | EZ Detect Colon Disease Test | BIOMERICA, INC. | KHE | 2020-07-01 |
| 00816917025063 | OC-Light S | POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC | KHE | 2020-04-20 |
| 00816917025087 | OC-Light S | POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC | KHE | 2020-04-20 |
| 00816917025056 | OC-Light S | POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC | KHE | 2020-03-20 |
| 10304040102517 | Henry Schein | HENRY SCHEIN, INC. | KHE | 2020-02-24 |