FDA UDI In Commercial Distribution 🇺🇸 United States

AXIEM™

DI: 00613994231031 · Model: 9733300 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AXIEM™
Primary DI
00613994231031
Version / Model
9733300
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-27
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
9808eed7-a945-441e-938a-60c5a4d41d52

Device Description

SHUNT PACK 9733300 AXIEM NON-INVASIVE

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45199 Multi-purpose stereotactic surgery system

Identifiers

Type ID
Primary 00613994231031

Customer Contacts