| Primary Device ID | 00810135960526 |
| NIH Device Record Key | efe784c9-091d-4d78-a43f-9cfb44db3ef5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Retropsoas Electrode |
| Version Model Number | ELEC1000-08 |
| Company DUNS | 047486041 |
| Company Name | NVISION BIOMEDICAL TECHNOLOGIES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com | |
| Phone | 210-598-5641 |
| diana@nvisionbiomed.com |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Height | 5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810135960526 [Primary] |
| ETN | Stimulator, Nerve |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-02 |
| Device Publish Date | 2023-10-25 |
| 00810135960564 | Retropsoas Electrode, NERVE CUFF TRIAL SIZER, 8/10MM. The EARP Nerve Cuff Electrode is used t |
| 00810135960557 | Retropsoas Electrode, NERVE CUFF TRIAL SIZER, 4/6MM. The EARP Nerve Cuff Electrode is used to |
| 00810135960540 | Retropsoas Electrode, NERVE CUFF APPLICATOR. The EARP Nerve Cuff Electrode is used to perform |
| 00810135960533 | Retropsoas Electrode, NERVE CUFF ELECTRODE, 10MM The EARP Nerve Cuff Electrode is used to per |
| 00810135960526 | Retropsoas Electrode, NERVE CUFF ELECTRODE, 8MM The EARP Nerve Cuff Electrode is used to perf |
| 00810135960519 | Retropsoas Electrode, NERVE CUFF ELECTRODE, 6MM The EARP Nerve Cuff Electrode is used to perf |
| 00810135960502 | Retropsoas Electrode, NERVE CUFF ELECTRODE, 4MM The EARP Nerve Cuff Electrode is used to perf |