| Primary Device ID | H787LVTX55570 |
| NIH Device Record Key | bf311b87-8dc9-48b6-ad49-c4420463be2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vortex |
| Version Model Number | LVTX5557 |
| Company DUNS | 601994184 |
| Company Name | ANGIODYNAMICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com | |
| Phone | +1(518)795-1676 |
| dgreer@angiodynamics.com |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Needle Gauge | 18 Gauge |
| Lumen/Inner Diameter | 1.6 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Length | 53 Centimeter |
| Catheter Gauge | 9.6 French |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | H787LVTX55570 [Primary] |
| LJT | PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-17 |
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| H787P12105K0 | Lifeport Single Plastic Vascular Access Port System with Attached 9.6F x 76cm Silicone Catheter |
| H787LVTX55570 | Vortex VX Single Titanium Port System with Attachable 9.6F x 53cm Silicone Catheter |
| H787LVTX55550 | Vortex VX Single Titanium Port System with Attachable 7.2F x 53cm Silicone Catheter |
| H787LVTX50570 | Vortex MP Titanium Low Profile Implanted Port with Attachable 5F x 76cm Silicone Catheter and Tr |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
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Shenzhen Qingyan E-commerce Co., Ltd. 2024-11-30 |
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Inductotherm Corp. 2024-07-01 |
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Inductotherm Corp. 2024-07-01 |
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Rainwater Management Solutions, Inc. 2024-04-11 |
![]() VORTEX 98470532 not registered Live/Pending |
Swiss Madison LLC 2024-03-27 |
![]() VORTEX 98463057 not registered Live/Pending |
Hughes, Albert 2024-03-22 |
![]() VORTEX 98416098 not registered Live/Pending |
Melnor, Inc. 2024-02-22 |
![]() VORTEX 98414349 not registered Live/Pending |
ALTENLOH, BRINCK & CO. US, INC. 2024-02-21 |
![]() VORTEX 98380575 not registered Live/Pending |
Rosen's, Inc. 2024-01-29 |
![]() VORTEX 98368008 not registered Live/Pending |
Tao Zhang 2024-01-21 |
![]() VORTEX 98286304 not registered Live/Pending |
Jobar International, Inc. 2023-11-27 |
![]() VORTEX 98245004 not registered Live/Pending |
Carfield, Hanna 2023-10-29 |