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Eon Mini™

FDA UDI

Class III (US FDA UDI)

by Advanced Neuromodulation Systems

Identity

Trade Name
Eon Mini™ FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
Charger Accessory FDA UDI
Model / Reference
3720 FDA UDI
Description
Charger Accessory FDA UDI

Identifiers

Catalog Number
3720 FDA UDI
Primary DI / UDI-DI
05414734405324 FDA UDI
PMA Number
P010032 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Noninvasive device battery charger 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Noninvasive device battery charger

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

Similar devices

Also classified as Noninvasive device battery charger.

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 9101be96-80ae-40b2-b421-0dad21596cdb 37 fields · synced Jun 8, 2026