| Primary Device ID | 07290109270012 |
| NIH Device Record Key | f9d5c8e3-c5e7-4c20-82ce-ca894d27129d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UriCap Female Device |
| Version Model Number | C |
| Catalog Number | FPR02020L |
| Company DUNS | 600502332 |
| Company Name | TILLA CARE LTD |
| Device Count | 1 |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290109270012 [Primary] |
| NZU | Collector, Urine, Powered, Non Indwelling Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-08 |
| Device Publish Date | 2019-12-31 |
| 07290109270203 - UriCap Base kit+ box of 30 | 2024-04-10 |
| 07290109270210 - UriCap Female + | 2024-04-10 |
| 07290109270227 - Home Sample Kits (box of 5) | 2024-04-10 |
| 07290109270234 - Home Base Kit (30-Day Supply) | 2024-04-10 |
| 07290109270197 - Tube Connector | 2023-10-10 |
| 07290109270173 - UriCap Base kit box of 30 | 2022-06-22 |
| 07290109270180 - UriCap Base kit box of 5 | 2022-06-22 |
| 07290109270135 - Urine bag - Tilla 2L | 2022-02-14 |