FDA UDI In Commercial Distribution 🇺🇸 United States

BioFlo Vortex

DI: 15051684017145 · Model: H787CT80LPBDNFVI0 · Angiodynamics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioFlo Vortex
Primary DI
15051684017145
Version / Model
H787CT80LPBDNFVI0
Catalog Number
CT80LPBDNFVI
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
04ac3bed-3d20-481b-9e7d-e0ba329b3597

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 H787CT80LPBDNFVI0
Primary 15051684017145

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190559 000

Device Sizes

Type Value Unit Text
Outer Diameter 2.67 Millimeter
Length 63 Centimeter
Catheter Gauge 8 French