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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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dOFM Push Tubing X Channel — 2 UDI-DI variants, MDR

MD Atlas
JOANNEUM RESEARCH Forschungsgesellschaft mbH

Data from EUDAMED, last updated May 23, 2026

dOFM Push Tubing X Channel

912012209PSHDF

2 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: JOANNEUM RESEARCH Forschungsgesellschaft mbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912012209PSHDF
Device name: dOFM Push Tubing X Channel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: JOANNEUM RESEARCH Forschungsgesellschaft mbH
SRN: AT-MF-000017155
Country: Austria
Email: health@joanneum.at
Phone: +43 316 876-4000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J2XPKKQWD8QAS5JG713ACEBY

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

dOFM Push Tubing 3-Channel09120122090022
dOFM Push Tubing 4-Channel09120122090039