# Unicen 21

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

- Canonical page: <https://devicerts.com/devices/unicen-21-ce-126ivd>
- Manufacturer: [Álvarez Redondo, S.A.](https://devicerts.com/manufacturers/alvarez-redondo-sa) (Spain)
- Device class: Class A (EU IVDR)
- EMDN: W02069003 CENTRIFUGES

## Registrations and authorizations

- **EUDAMED** · CE/IVDR · European Union · Basic UDI-DI 843661198-IVD-UNI1-JZ · registered 2024-12-10 · status: Active

## Recalls

No recall on record.

## Identity

- Model / reference: CE 126IVD [EUDAMED]; CE 127IVD [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 08436611980202 [EUDAMED]; 08436611980219 [EUDAMED]
- Basic UDI-DI: 843661198-IVD-UNI1-JZ [EUDAMED]
- EMDN code: W02069003 [EUDAMED]

## Classification

- Device class: Class A [EUDAMED]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Spain [EUDAMED]

## Properties

- IVD instrument: Yes [EUDAMED]
- Supplied sterile: No [EUDAMED]
- Sterilise before use: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains substances of microbial origin: No [EUDAMED]
- Reagent: No [EUDAMED]
- IVD kit: No [EUDAMED]
- Self-testing: No [EUDAMED]
- Near-patient testing: No [EUDAMED]
- Professional testing: No [EUDAMED]
- Companion diagnostics: No [EUDAMED]
- New device: No [EUDAMED]

## Source and citation

- Cite as: Unicen 21, Álvarez Redondo, S.A. deviCERTS medical device catalogue. https://devicerts.com/devices/unicen-21-ce-126ivd (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/unicen-21-ce-126ivd.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/unicen-21-ce-126ivd
- 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.