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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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REHAVISTA Talk Pad — 3 UDI-DI variants, MDR (REHAVISTA GmbH)

MD Atlas
REHAVISTA GmbH

Data from EUDAMED, last updated May 23, 2026

REHAVISTA Talk Pad

PP103951913324170

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: REHAVISTA GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: PP103951913324170
Device name: REHAVISTA Talk Pad
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: REHAVISTA GmbH
SRN: DE-MF-000005403
Country: Germany
Email: info@rehavista.de
Phone: 049 421 989 628 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KG01SN5ZTX0HQ7JMPJMV9FR0

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

R05249PP10395R0524920
R05247PP10395R0524789
R05251PP10395R0525118