# NeoGen Footswitch

> Active: European Union. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/neogen-footswitch-230-027>
- Manufacturer: [Energist](https://devicerts.com/manufacturers/energist) (United Kingdom)
- Device class: Class I (EU MDD / EU MDR); Class IIb (EU MDD / EU MDR)
- EMDN: Z12040203 DERMAL REGENERATION EQUIPMENT

## Registrations and authorizations

- **EUDAMED** · CE/MDD · European Union · Basic UDI-DI 506044052NeoGen-NF-001JC · UDI-DI 05060440520365 · registered 2026-04-14 · status: Active
- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 506044052NeoGen-NF-001JC · UDI-DI 05060440520365 · registered 2026-04-14 · status: Active

## Recalls

No recall on record.

## Identity

- Trade name: NeoGen Footswitch [EUDAMED]; NeoGen [EUDAMED]
- Model / reference: 230-027 [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 05060440520365 [EUDAMED]
- Basic UDI-DI: 506044052NeoGen-NF-001JC [EUDAMED]; B-05060440520365 [EUDAMED]
- EMDN code: Z12040203 [EUDAMED]

## Classification

- Device class: Class I [EUDAMED]; Class IIb [EUDAMED]
- EU registration type: Standard device [EUDAMED]; Legacy device (under a directive) [EUDAMED]
- EU market of registration: Netherlands [EUDAMED]

## Properties

- Supplied sterile: No [EUDAMED]
- Sterilise before use: No [EUDAMED]
- Implantable: No [EUDAMED]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]

## Source and citation

- Cite as: NeoGen Footswitch, Energist. deviCERTS medical device catalogue. https://devicerts.com/devices/neogen-footswitch-230-027 (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/neogen-footswitch-230-027.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/neogen-footswitch-230-027
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.