FDA UDI In Commercial Distribution 🇺🇸 United States

Mi-Axus Catheter

DI: B293MIA9095S0 · Model: MIA9095S · MIVI NEUROVASCULAR
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mi-Axus Catheter
Primary DI
B293MIA9095S0
Version / Model
MIA9095S
Company Name
MIVI NEUROVASCULAR
Labeler DUNS
076836823
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-23
Public Version
7
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
f9bd2ebd-ba09-4b84-b208-f3be4fee962c

Device Description

The Mi-Axus 8F Guide Catheter is a single lumen, braided, variable stiffness shaft catheter designed for use in facilitating the insertion and guidance of micro catheters into a selected blood vessel in the peripheral, coronary, or neuro vascular system. A radiopaque marker is included on the distal end. The catheter shaft has a hydrophilic coating. The proximal segment is constructed with Vestamid. The distal segment of the PEBAX is impregnated with barium sulphate for increased radiopacity.

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
DQY Catheter, Percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary B293MIA9095S0

Premarket Submissions

Submission Number Supplement Number
K151396 000

Device Sizes

Type Value Unit Text
Length 95 Centimeter
Catheter Gauge 8 French