Primary Device ID | 07460691956209 |
NIH Device Record Key | a2dbd3ee-110b-4b1e-892d-e46ac07a0a08 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRUWAVE, VAMP |
Version Model Number | PXVK0995 |
Catalog Number | PXVK0995 |
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 |
Length | 97.5 Inch |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A COOL, DRY PLACE. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07460691956209 [Primary] |
GS1 | 57460691956204 [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 | 2018-07-06 |
Device Publish Date | 2016-09-03 |
00690103162141 | PRESSURE MONITORING SET |
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