FDA UDI In Commercial Distribution 🇺🇸 United States

NeuroSphere™

DI: 05415067046956 · Model: 3874 · ST. JUDE MEDICAL, INC.
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NeuroSphere™
Primary DI
05415067046956
Version / Model
3874
Catalog Number
3874
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-01
Public Version
1
Public Version Date
2022-09-09
Public Version Status
New
Public Device Record Key
2df5d0dd-b65d-4deb-9bbe-9c2e4a4dd65b

Device Description

Clinician Programmer

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
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
61393 Multiple active implantable device programmer

Identifiers

Type ID
Previous 05415067023674
Primary 05415067046956

Customer Contacts