FDA UDI In Commercial Distribution 🇺🇸 United States

Axium™

DI: 05415067027344 · Model: MN12050 · SPINAL MODULATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Axium™
Primary DI
05415067027344
Version / Model
MN12050
Catalog Number
MN12050
Company Name
SPINAL MODULATION, INC.
Labeler DUNS
617312272
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e4ff0942-4744-481b-9661-dddd18b7a150

Device Description

Lead Accessories 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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PMP Dorsal root ganglion stimulator for pain relief

GMDN Terms

Code Name
44063 Neurosurgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 05415067027344

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P150004 002

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry.
Type
Storage Environment Temperature
Temperature Range
14 – 122 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
14 – 122 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius