| Primary Device ID | 00860007896965 |
| NIH Device Record Key | c7ed02bb-e201-43a5-8b47-0576e0e0ecd4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | eCoin Patient Kit |
| Version Model Number | 1011-1901 |
| Company DUNS | 968538988 |
| Company Name | Valencia Technologies Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860007896965 [Primary] |
| QPT | Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-06 |
| Device Publish Date | 2022-04-28 |
| 00860007896972 - eCoin External Controller Kit | 2023-05-05 eCoin External Controller Kit |
| 00860007896903 - eCoin Device Kit | 2022-05-06 eCoin Device Kit |
| 00860007896910 - eCoin External Controller Kit | 2022-05-06 eCoin External Controller Kit |
| 00860007896927 - eCoin Procedural Kit | 2022-05-06 eCoin Procedural Kit |
| 00860007896941 - eCoin Aftercare Kit | 2022-05-06 eCoin Aftercare Kit |
| 00860007896958 - eCoin Explant Kit | 2022-05-06 eCoin Explant Kit |
| 00860007896965 - eCoin Patient Kit | 2022-05-06eCoin Patient Kit |
| 00860007896965 - eCoin Patient Kit | 2022-05-06 eCoin Patient Kit |