CarePath System
The CarePath system facilitates evaluations measuring urine output. It consists of the CarePath device, accompanying documents, and training. The system: • Measures and calculates flow rate…
The CarePath system facilitates evaluations measuring urine output. It consists of the CarePath device, accompanying documents, and training. The system: • Measures and calculates flow rate and volume from urination data • Automatically transmits urination data to a secure location • Creates and provides uroflow reports to healthcare providers The intended operator of the CarePath device is the patient. The CarePath system has no user-serviceable components. This system is not to be serviced or maintained by the user. The intended environments are hospitals, clinics, doctor’s offices and the patient’s home.
Who Else Makes It
Concentrated in Jiangsu (2), Guangdong (2), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Dongguan BAO Kang Dian ZI KE JI Limited | Dongguan | Guangdong | Contract manufacturer | 24 |
| Primecare Medical (Suzhou) Co., Ltd. | Changshu | Jiangsu | Contract manufacturer | 20 |
| Changshu Rozer Sterilization Technology Co., Ltd. | Changshu | Jiangsu | Contract manufacturer | 43 |
| Hangzhou Primecare Medical Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 29 |
| Amsino Medical (Shanghai) Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 22 |
| Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd. | Guangzhou | Guangdong | Manufacturer | 4 |
| Qingdao Unison Industries Co., Limited | Shandong | Shandong | Specification developer | 3 |
Record
| Listed by | I/O Urology Corporation, United States |
|---|---|
| FDA product code | EXY |
| Device type | Uroflowmeter |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1800 |
| Establishment | Specification developer, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2024-06-20 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date |
| Storage | Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 15 to 93 % RH; Handling environment temperature 5 to 40 °C; Storage environment atmospheric pressure 70 to 106 KiloPascal; Storage environment humidity 15 to 93 % RH; Storage environment temperature -20 to 60 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DCDUFD-001M | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| CarePath | Cleartrac Technologies, LLC | 5 |
| Fize kUO Console | Fize Research Ltd | 5 |
| Urocap IV Light | Laborie Medical Technologies, Canada ULC | 4 |
| proudP | Soundable Health, Inc. | 2 |
| Fize kUO Disposable Kit | Fize Research Ltd | 2 |
| Urocap III | Laborie Medical Technologies, Canada ULC | 2 |
| Stream Dx | Zien Medical Technologies LLC | 2 |
| Rivus | Neurosoft, OOO | 2 |
| Fize kUO Disposable kit Pediatrics | Fize Research Ltd | 2 |
| EasyFlo Console | Srs Medical Systems, Inc. | 1 |
| EasyFlo Scale | Srs Medical Systems, Inc. | 1 |
| WiFLOW | Prometheus Group OF NEW Hampshire Limited, THE | 1 |
Showing 12 of 30. All products under Uroflowmeter
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.