Primary Device ID | 03085252800537 |
NIH Device Record Key | c19bb660-869e-4e59-9918-1978984c16bf |
Commercial Distribution Discontinuation | 2017-12-13 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Extended Length ViperWire Advance |
Version Model Number | VPR-GW-EL14 |
Company DUNS | 024954518 |
Company Name | Cardiovascular Systems, Inc. |
Device Count | 5 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03085252800537 [Package] Contains: 10852528005381 Package: Box [5 Units] Discontinued: 2017-12-13 Not in Commercial Distribution |
GS1 | 10852528005381 [Primary] |
GS1 | 10852528005404 [Unit of Use] |
MCW | Catheter, Peripheral, Atherectomy |
Steralize Prior To Use | true |
Device Is Sterile | true |
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
[03085252800537]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-10 |
Device Publish Date | 2017-09-07 |
03085252800537 | ViperWire, Advance, Extended Length, Peripheral, 0.014" Dia spring tip, 475cm, 5 Pack |
30852528005743 | ViperWire, Advance, Flex Tip, Extended Length, Peripheral, 0.018" Dia spring tip, 475cm, 5 Pack |
30852528005736 | ViperWire, Advance, , Flex Tip, Extended Length, Peripheral, 0.014" Dia spring tip, 475cm, 5 Pac |
10852528005466 | ViperWire, Advance, Extended Length, Peripheral, 0.018" Dia spring tip, 475cm, 5 Pack |
30852528005453 | ViperWire, Advance, Extended Length, Peripheral, 0.014" Dia spring tip, 475cm, 5 Pack |
30852528005392 | ViperWire, Advance, Extended Length, Peripheral, 0.018" Dia spring tip, 475cm, 5 Pack |