FDA UDI Not in Commercial Distribution 🇺🇸 United States

Vortex

DI: H787LVTX75130 · Model: LVTX7513 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vortex
Primary DI
H787LVTX75130
Version / Model
LVTX7513
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-07
Public Version
4
Public Version Date
2021-11-30
Public Version Status
Update
Public Device Record Key
ec0f6322-7028-4050-8b36-85e4f2a6e1ab
Distribution End Date
2021-11-23

Device Description

Vortex LP Single Plastic Port System with Attachable 8.4F x 76cm Polyurethane 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 H787LVTX75130

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010767 000

Device Sizes

Type Value Unit Text
Needle Gauge 18 Gauge
Lumen/Inner Diameter 1.6 Millimeter
Catheter Gauge 8.4 French
Outer Diameter 2.8 Millimeter
Length 76 Centimeter