FDA UDI Not in Commercial Distribution 🇺🇸 United States

BioFlo Vortex

DI: H787CT50LPBAVI0 · Model: CT50LPBAVI · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BioFlo Vortex
Primary DI
H787CT50LPBAVI0
Version / Model
CT50LPBAVI
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-29
Public Version
2
Public Version Date
2024-11-18
Public Version Status
Update
Public Device Record Key
5661bb34-2b5c-4250-856e-23bf00853aa7
Distribution End Date
2024-11-15

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
Primary H787CT50LPBAVI0

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