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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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Coaxial Interventional Needle — 31 UDI-DI variants, MDR

MD Atlas
ITP Innovative Tomography Products GmbH

Data from EUDAMED, last updated May 23, 2026

Coaxial Interventional Needle

426241068KIRKIM94

31 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: ITP Innovative Tomography Products GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426241068KIRKIM94
Device name: Coaxial Interventional Needle
Device model: Coaxial Interventional Needle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: ITP Innovative Tomography Products GmbH
SRN: DE-MF-000008634
Country: Germany
Email: info@innotom.com
Phone: +49 234 54621940

Variants by status

UDI-DI variants

31 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9MGD4YNCW24A52F9WX5QFN

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

KIM22/1504262410680081
KIM20/1504262410680128
KIM20/1004262410680104
KIM18/15T04262410680241
KIM18/1004262410680166
KIM20/2004262410680142

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