FDA UDI Not in Commercial Distribution 🇺🇸 United States

BioFlo

DI: H965440280 · Model: 44028 · 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
H965440280
Version / Model
44028
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-09
Public Version
5
Public Version Date
2024-09-23
Public Version Status
Update
Public Device Record Key
6b95eb27-11c4-4a03-a113-4c50980ea4ed
Distribution End Date
2024-09-20

Device Description

BioFlo Dual Port with Endexo Technology - Plastic Port with Filled Suture Holes and 8F Polyurethane Catheter

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 H965440280

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French
Pressure 300 Pound per Square Inch
Needle Gauge 18 Gauge
Device Size Text, specify Dual Lumen
Outer Diameter 2.6 Millimeter
Length 63 Centimeter