FDA UDI In Commercial Distribution 🇺🇸 United States

BioFlo

DI: 15051684029988 · Model: H965460320 · Angiodynamics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioFlo
Primary DI
15051684029988
Version / Model
H965460320
Catalog Number
46-032
Company Name
Angiodynamics, Inc.
Labeler DUNS
079252781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-18
Public Version
1
Public Version Date
2025-03-26
Public Version Status
New
Public Device Record Key
c347d3f1-f817-4b90-a933-a58191124ba5

Device Description

BioFlo Midline with ENDEXO Technology 3F SL-10cm AST - Rapid Deployment Procedure Basic Kit

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
Labeling does not contain MRI Safety Information
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
64574 Peripheral intravenous cannula

Identifiers

Type ID
Package 25051684029985
Primary 15051684029988

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 1.02 Millimeter
Lumen/Inner Diameter 0.018 Inch
Length 10 Centimeter
Catheter Gauge 3 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius