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NeuroSphere™

FDA UDI

Class III (US FDA UDI)

by Advanced Neuromodulation Systems

Identity

Trade Name
NeuroSphere™ FDA UDI
Generic Name
Multiple active implantable device programmer FDA UDI
Device Name
Digital Health App FDA UDI
Model / Reference
3876 FDA UDI
Description
Digital Health App FDA UDI

Identifiers

Catalog Number
3876 FDA UDI
Primary DI / UDI-DI
05415067050311 FDA UDI
PMA Number
P010032 FDA UDI
P140009 FDA UDI
P150004 FDA UDI
FDA Product Code
MHY FDA UDI
PMP FDA UDI
LGW FDA UDI
NHL FDA UDI
PJS FDA UDI
GMDN Term
Multiple active implantable device programmer FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple active implantable device programmer

NeuroSphere™ by Advanced Neuromodulation Systems — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple active implantable device programmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e76891fd-6f54-4a34-a152-1ea2d74ec860 36 fields · synced May 30, 2026