FDA UDI In Commercial Distribution 🇺🇸 United States

BioFlo

DI: H965461900 · Model: 46190 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
BioFlo
Primary DI
H965461900
Version / Model
46190
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
6
Public Version Date
2021-06-28
Public Version Status
Update
Public Device Record Key
07aa4c17-9c6e-406c-8e0c-7d97bf67bbf0

Device Description

BioFlo Midline with ENDEXO Technology Catheter 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
Primary H965461900
Secondary 15051684025300

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 3 French
Outer Diameter 1.02 Millimeter
Length 20 Centimeter