Primary Device ID | 07460691944824 |
NIH Device Record Key | 7aec15f9-4c1c-46e0-a45d-911decfccf79 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VAMP PLUS |
Version Model Number | VP1 |
Catalog Number | VP1 |
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 | 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 |
Length | 60 Inch |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A COOL, DRY PLACE. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07460691944824 [Primary] |
GS1 | 57460691944829 [Package] Package: Shipper [10 Units] In Commercial Distribution |
KRA | Catheter, continuous flush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-28 |
Device Publish Date | 2016-09-03 |
07460691958616 | BLOOD MANAGEMENT SYSTEM |
07460691955578 | VAMP PLUS KIT - STERILE |
07460691944831 | BLOOD MANAGEMENT SYSTEM |
07460691944824 | BLOOD MANAGEMENT SYSTEM. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VAMP PLUS 75344794 2282031 Live/Registered |
Edwards Lifesciences Corporation 1997-08-21 |