Eon Mini™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name: Eon Mini™ FDA UDI
Generic Name: Noninvasive device battery charger FDA UDI
Model / Reference: 3718 FDA UDI

Identifiers

Catalog Number: 3718 FDA UDI
Primary DI / UDI-DI: 05414734402606 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 36 Inch FDA UDI

Category: Noninvasive device battery charger

Eon Mini™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: St. Jude Medical, Inc.

Sources (1)

FDA UDI f6af4caa-19b2-4eb1-bf5e-a71780cd239d 37 fields · synced Jun 1, 2026