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Axonics

FDA UDI

Class III (US FDA UDI)

by Axonics Modulation Technologies, Inc.

Identity

Trade Name
Axonics FDA UDI
Generic Name
Implant battery charger FDA UDI
Device Name
Charging Device FDA UDI
Model / Reference
1401 FDA UDI
Description
Charging Device FDA UDI

Identifiers

Catalog Number
1401 FDA UDI
Primary DI / UDI-DI
10810005340387 FDA UDI
FDA Product Code
QON FDA UDI
EZW FDA UDI
GMDN Term
Implant battery charger FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
876.5270 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Implant battery charger

Axonics by Axonics Modulation Technologies, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implant battery charger.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e6d77f3-a7fc-463b-ab44-0b01007f598c 35 fields · synced May 30, 2026