FDA UDI Not in Commercial Distribution 🇺🇸 United States

Vortex

DI: H787LVTX55550 · Model: LVTX5555 · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vortex
Primary DI
H787LVTX55550
Version / Model
LVTX5555
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
601994184
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
4
Public Version Date
2021-11-30
Public Version Status
Update
Public Device Record Key
d94b78fb-765e-4c7d-bc17-d991c7dd96d7
Distribution End Date
2021-11-23

Device Description

Vortex VX Single Titanium Port System with Attachable 7.2F x 53cm Silicone Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
61494 Vascular port/catheter

Identifiers

Type ID
Primary H787LVTX55550

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010767 000

Device Sizes

Type Value Unit Text
Length 53 Centimeter
Needle Gauge 18 Gauge
Outer Diameter 2.4 Millimeter
Catheter Gauge 7.2 French
Lumen/Inner Diameter 1.3 Millimeter