FDA UDI In Commercial Distribution 🇺🇸 United States

BioFlo

DI: H965440230 · Model: 44023 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioFlo
Primary DI
H965440230
Version / Model
44023
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2021-05-24
Public Version Status
Update
Public Device Record Key
68bf950d-7642-42ad-8454-04f85d5f195f

Device Description

BioFlo Titanium Port with PASV Valve Technology (Non-Filled Suture Holes) and 6F x 63cm Polyurethane Catheter with ENDEXO 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 H965440230
Secondary 15051684018753

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 6 French
Outer Diameter 2.1 Millimeter
Pressure 300 Pound per Square Inch
Length 63 Centimeter
Lumen/Inner Diameter 1.3 Millimeter
Needle Gauge 18 Gauge