FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mi-Axus Catheter

DI: B293MIA90900 · Model: MIA9090 · MIVI NEUROVASCULAR
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mi-Axus Catheter
Primary DI
B293MIA90900
Version / Model
MIA9090
Company Name
MIVI NEUROVASCULAR
Labeler DUNS
076836823
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
7
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
f3381bed-2c3a-4af8-b377-0513a4f3f474
Distribution End Date
2018-12-07

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 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 B293MIA90900

Premarket Submissions

Submission Number Supplement Number
K151396 000

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French
Length 90 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Dark and dry