| Primary Device ID | 00690103198966 |
| NIH Device Record Key | 16e3acf5-2730-40e3-bb55-96038cc3e45d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FloTrac, VAMP Optima |
| Version Model Number | MHD8VZ |
| Catalog Number | MHD8VZ |
| Company DUNS | 134139174 |
| Company Name | Edwards Lifesciences LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | 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 |
| Length | 84 Inch |
| Length | 84 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00690103198966 [Primary] |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-30 |
| Device Publish Date | 2018-10-30 |
| 50690103200206 | FloTrac sensor with VAMP Optima system |
| 50690103198992 | FloTrac sensor with VAMP Optima system |
| 00690103198980 | FloTrac sensor with VAMP Optima system |
| 50690103198978 | FloTrac sensor with VAMP Optima system |
| 00690103198966 | FloTrac sensor with VAMP Optima system |