Viance VNC-FX-150
GUDID 00821684052716
Crossing Catheter Flexible
Covidien LP
Vascular guide-catheter, single-use| Primary Device ID | 00821684052716 |
| NIH Device Record Key | f5cb40a2-22b9-43d8-a599-4e4b053dfc14 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Viance |
| Version Model Number | VNC-FX-150 |
| Catalog Number | VNC-FX-150 |
| Company DUNS | 968903703 |
| Company Name | Covidien LP |
| 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 | 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 |
Customer Support Contacts
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
Device Dimensions
| Catheter Gauge | 5 French |
| Catheter Gauge | 5 French |
| Catheter Gauge | 5 French |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
| Device Size Text, specify | 0 |
| Catheter Gauge | 5 French |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00821684052716 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120533
FDA Product Code
| DQY | CATHETER, PERCUTANEOUS |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-01-23 |
| Device Publish Date | 2015-10-12 |
On-Brand Devices [Viance]
| 00821684052723 | Crossing Catheter Standard |
| 00821684052716 | Crossing Catheter Flexible |
Trademark Results [Viance]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VIANCE 87474744 not registered Dead/Abandoned |
BofI Federal Bank 2017-06-05 |
 VIANCE 85844912 4439025 Live/Registered |
Covidien, LP 2013-02-08 |
 VIANCE 85843879 not registered Dead/Abandoned |
Lady Americana Associates, Inc. 2013-02-07 |
 VIANCE 85767128 4483473 Live/Registered |
THE ALKALINE RESEARCH GROUP, LLC 2012-10-30 |
 VIANCE 85631481 not registered Dead/Abandoned |
COVIDIEN LP 2012-05-22 |
 VIANCE 77508165 3871871 Dead/Cancelled |
DELL INC. 2008-06-25 |
 VIANCE 77058313 3640088 Live/Registered |
Viance, LLC 2006-12-06 |
 VIANCE 74169450 1754524 Dead/Cancelled |
LADY AMERICANA ASSOCIATES, INC. 1991-05-23 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.