FDA UDI Not in Commercial Distribution 🇺🇸 United States

BioFlo

DI: H965440150 · Model: 44015 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BioFlo
Primary DI
H965440150
Version / Model
44015
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2024-09-23
Public Version Status
Update
Public Device Record Key
e3654773-d790-4d01-965e-a6901dc133a7
Distribution End Date
2024-09-20

Device Description

BioFlo Titanium Port with 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 H965440150

Customer Contacts

Device Sizes

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