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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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RUN700/T — 12 UDI-DI variants, MDR (RUNNER SRL)

MD Atlas
RUNNER SRL

Data from EUDAMED, last updated May 31, 2026

RUN700/T

805383912FT01CF

12 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: 805383912FT01CF
Device name: RUN700/T
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 14, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7GR5MZZSHFDW4812HNZ5QY3

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

RUN1400/T configurazione B08053839123237
RUN1400/T08053839120168
RUN1400/TR configurazione C08053839123275
RUN1400/TR08053839120175
RUN1400/TR configurazione D08053839123213
RUN1400/TR configurazione B08053839123251
RUN700/T configurazione B08053839123220
RUN700/TR configurazione D08053839123206
RUN700/TR configurazione B08053839123244
RUN700/TR configurazione C08053839123268
RUN700/TR08053839120151
RUN700/T08053839120144