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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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RUN2011/TR-PC — 334 UDI-DI variants, MDR (RUNNER SRL)

MD Atlas
RUNNER SRL

Data from EUDAMED, last updated May 31, 2026

RUN2011/TR-PC

805383912FT02CH

334 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RUNNER SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805383912FT02CH
Device name: RUN2011/TR-PC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: RUNNER SRL
SRN: IT-MF-000029314
Country: Italy
Email: piero@runneritaly.it
Phone: +39053558447

Variants by status

UDI-DI variants

334 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K82Z1FRSYHYGFGKEE0VDZRTM

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

XR600P configurazione J08053839122285
XR600P configurazione I08053839122162
XR600P configurazione K08053839122346
XR600P configurazione S08053839122469
XR600P configurazione Q08053839122490
XR600P configurazione C08053839121806
XR600P08053839120267
XR600R08053839120243
XR600R configurazione B08053839121561