FDA UDI In Commercial Distribution 🇺🇸 United States

Axium™

DI: 05415067025630 · Model: MN23400 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Axium™
Primary DI
05415067025630
Version / Model
MN23400
Catalog Number
MN23400
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-29
Public Version
4
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
c508ae04-62a3-4b36-958b-363a835d980a

Device Description

Programmer Charger Kit For use with Clinical Programmer MN10700

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PMP Dorsal root ganglion stimulator for pain relief

GMDN Terms

Code Name
17115 Noninvasive device battery charger

Identifiers

Type ID
Primary 05415067025630

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P150004 000
P150004 005

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry.