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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

R05250 — Class I MDR by REHAVISTA GmbH

MD Atlas
REHAVISTA GmbH

EUDAMED last updated this device on Feb 4, 2026

R05250

PP103951913325803

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: REHAVISTA GmbH
UDI-DI code: PP10395R0525004
Reference / catalog number: R05250

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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 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: PP10395R0525004
Basic UDI-DI: PP103951913325803
Reference / catalog number: R05250
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 - 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-metatalkde
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

R04885PP103951913326451On the market R04893PP103951913326451On the market R04877PP103951913326451On the market R05249PP103951913324170On the market R05247PP103951913324170On the market

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.