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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

R05248 — Class I MDR by REHAVISTA GmbH

MD Atlas
REHAVISTA GmbH

EUDAMED last updated this device on Feb 4, 2026

R05248

PP103951913325803

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: REHAVISTA GmbH
UDI-DI code: PP10395R0524806
Reference / catalog number: R05248

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Manufacturer information

Organization name: REHAVISTA GmbH
SRN: DE-MF-000005403
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: PP10395R0524806
Basic UDI-DI: PP103951913325803
Reference / catalog number: R05248
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Highlights auf einen Blick - benutzerfreundliches und modernes Design - robust und zuverlässig - zehn Stunden Akkulaufzeit - große und leicht zu bedienende Tasten - Schutzart IP 22 - Tragegurt - sichere Befestigungsmöglichkeiten (optional) - Fingerführungen, wahlweise mit farbigem Cover (optional); Weitere Informationen: - Dynamisches Display: 10,9" - Gewicht: 840 g - Symbolbasierte Software (GoTalk NOW) - METACOM-Symbole enthalten - Synthetische Stimmen (weibl./männl.) - mit Antireflexfolie versehen - Komplettinstallation, Funktionsprüfung - Support-Hotline - Gewährleistungs- und Reparaturannahme/-Abwicklung
Additional information URL: https://www.rehavista.de/shop/artikel/talk-pad-slimline-mit-gotalk-now
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y214209ALPHABETIC AND SYMBOLIC COMMUNICATORS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.