| Primary Device ID | 00860003114704 |
| NIH Device Record Key | 60927dc4-fe13-480c-8f9c-270d96425e05 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CarePath |
| Version Model Number | DCD-001F |
| Company DUNS | 082296929 |
| Company Name | Cleartrac Technologies, LLC |
| Device Count | 16 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860003114704 [Unit of Use] |
| GS1 | 10860003114701 [Primary] |
| EXY | Uroflowmeter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-07-08 |
| Device Publish Date | 2021-06-30 |
| 00860003114742 | Base Station (Charger) |
| 00860003114735 | MALE Urine Flow Disposable |
| 00860003114728 | FEMALE Urine Flow Disposable |
| 00860003114711 | MALE Urine Flow Device |
| 00860003114704 | FEMALE Urine Flow Device |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CAREPATH 98629842 not registered Live/Pending |
Christopher Lewis 2024-07-02 |
![]() CAREPATH 90865095 not registered Live/Pending |
Homesteaders Life Company 2021-08-04 |
![]() CAREPATH 88044266 not registered Live/Pending |
ClearTrac Technologies, LLC 2018-07-19 |
![]() CAREPATH 87706986 not registered Live/Pending |
Homesteaders Life Company 2017-12-04 |
![]() CAREPATH 87223600 5897554 Live/Registered |
Senderra Rx Partners, LLC 2016-11-02 |
![]() CAREPATH 85575288 4611982 Live/Registered |
Laboratory Corporation of America Holdings 2012-03-21 |
![]() CAREPATH 75827062 not registered Dead/Abandoned |
Dianon Systems, Inc 1999-10-20 |
![]() CAREPATH 75827059 not registered Dead/Abandoned |
Dianon Systems, Inc 1999-10-20 |
![]() CAREPATH 75150705 2442916 Live/Registered |
LABORATORY CORPORATION OF AMERICA HOLDINGS 1996-08-02 |
![]() CAREPATH 75150704 2427187 Live/Registered |
LABORATORY CORPORATION OF AMERICA HOLDINGS 1996-08-02 |