FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 05415067054111 · Model: 1210 · ADVANCED NEUROMODULATION SYSTEMS, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
05415067054111
Version / Model
1210
Catalog Number
1210
Company Name
ADVANCED NEUROMODULATION SYSTEMS, INC.
Labeler DUNS
021675699
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-02
Public Version
1
Public Version Date
2026-03-10
Public Version Status
New
Public Device Record Key
9ddca4a2-040b-4290-9b84-0beaed213426

Device Description

Patient Magnet

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LGW Stimulator, spinal-cord, totally implanted for pain relief
PMP Dorsal root ganglion stimulator for pain relief
MHY Stimulator, electrical, implanted, for parkinsonian tremor
NHL Stimulator, electrical, implanted, for parkinsonian symptoms
PJS Stimulator, electrical, implanted, for essential tremor

GMDN Terms

Code Name
57996 Active implantable device control magnet

Identifiers

Type ID
Primary 05415067054111

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010032 243
P140009 124
P150004 090