| Primary Device ID | 00690103032444 |
| NIH Device Record Key | 51c84e20-88ba-4518-b963-42d7ff7ddb6e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Edwards Lifesciences Femoral Venous Cannula |
| Version Model Number | LV89528 |
| Catalog Number | LV89528 |
| Company DUNS | 134139174 |
| Company Name | Edwards Lifesciences LLC |
| 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 | +1(800)822-9637 |
| tech_support@edwards.com | |
| Phone | +1(800)822-9637 |
| tech_support@edwards.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00690103032444 [Primary] |
| GS1 | 50690103032449 [Package] Package: Shipper [10 Units] In Commercial Distribution |
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-31 |
| 00690103146684 | Femoral Venous Cannula |
| 00690103146677 | Femoral Venous Cannula |
| 00690103146660 | Femoral Venous Cannula |
| 00690103146653 | Femoral Venous Cannula |
| 00690103146646 | Femoral Venous Cannula |
| 00690103032451 | FEMORAL VENOUS CANNULA |
| 00690103032444 | Femoral Venous Cannula |