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EUDAMED last updated this device on Nov 4, 2025
805383912FT02CHPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →RUN7410/TR-PC configurazione M is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by RUNNER SRL. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →08053839122070Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →805383912FT02CHRUN7410/TR-PC configurazione MUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →(01)08053839122070
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z129006TREADMILLS FOR PHYSIOTHERAPY AND/OR DIAGNOSTIC USESSterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Germany | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market |
IT-MF-000029314Certificate health across this manufacturer's portfolio.
ITH 1344179 1IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →805383912FT02CHOn the marketREHARUNNER 02/70 PC configurazione M805383912FT02CHOn the marketREHARUNNER 02/70 PC configurazione H805383912FT02CHOn the marketREHARUNNER 02/70 PC configurazione E805383912FT02CHOn the marketREHARUNNER 02/70 PC configurazione K805383912FT02CHOn the market