Primary Device ID | 50690103199074 |
NIH Device Record Key | 819b65eb-17bb-4ef6-83a2-7670ae3e496b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VAMP Optima |
Version Model Number | VOPTIMAL |
Catalog Number | VOPTIMAL |
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 | 00690103199079 [Primary] |
GS1 | 50690103199074 [Package] Contains: 00690103199079 Package: Shipper [10 Units] In Commercial Distribution |
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 |
50690103199074 | VAMP Optima System |
50690103199067 | VAMP Optima System |