FDA UDI In Commercial Distribution 🇺🇸 United States

BioFlo Vortex

DI: 15051684016988 · Model: H787CT50LTBAVI0 · Angiodynamics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioFlo Vortex
Primary DI
15051684016988
Version / Model
H787CT50LTBAVI0
Catalog Number
CT50LTBAVI
Company Name
Angiodynamics, Inc.
Labeler DUNS
079252781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-19
Public Version
2
Public Version Date
2025-03-20
Public Version Status
Update
Public Device Record Key
3c38114d-1ed5-4e20-aeb6-917e67aca48e

Device Description

SmartPort+ Low Profile Port with Endexo and Vortex Technology

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
Previous H787CT50LTBAVI0
Primary 15051684016988

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190559 000

Device Sizes

Type Value Unit Text
Length 45 Centimeter
Catheter Gauge 5 French
Outer Diameter 1.8 Millimeter