| Primary Device ID | 00851616007545 |
| NIH Device Record Key | 73ab8c80-9a49-4cfa-965c-b3fafd02947f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Excipio LV |
| Version Model Number | EXC-2510-125 |
| Catalog Number | EXC-2510-125 |
| Company DUNS | 048268128 |
| Company Name | Contego Medical, 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com | |
| Phone | +1-800-708-7271 |
| info@contegomedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851616007545 [Primary] |
| QEW | Peripheral Mechanical Thrombectomy With Aspiration |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-10-02 |
| Device Publish Date | 2023-09-23 |
| 00851616007583 - Neuroguard IEP® System | 2024-10-31 The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent • A delivery catheter which in |
| 00851616007590 - Neuroguard IEP® System | 2024-10-31 The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent • A delivery catheter which in |
| 00851616007606 - Neuroguard IEP® System | 2024-10-31 The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent • A delivery catheter which in |
| 00851616007613 - Neuroguard IEP® System | 2024-10-31 The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent • A delivery catheter which in |
| 00851616007545 - Excipio LV | 2023-10-02The Excipio LV Thrombectomy Device is indicated for the non-surgical removal of emboli and thrombi from peripheral blood vessels. |
| 00851616007545 - Excipio LV | 2023-10-02 The Excipio LV Thrombectomy Device is indicated for the non-surgical removal of emboli and thrombi from peripheral blood vessels |
| 00851616007149 - Vanguard | 2023-09-13 The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is indicated for percutaneous translum |
| 00851616007156 - Vanguard | 2023-09-13 The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is indicated for percutaneous translum |
| 00851616007293 - Paladin | 2023-09-13 The Paladin Carotid PTA Balloon System with Integrated Embolic Protection (IEP), is indicated for Percutaneous Transluminal Angi |