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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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Extensions — 5 UDI-DI variants, MDR (IT-V Medizintechnik GmbH)

MD Atlas
IT-V Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Extensions

91200743939ME

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: IT-V Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 91200743939ME
Device name: Extensions
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: IT-V Medizintechnik GmbH
SRN: AT-MF-000001918
Country: Austria
Email: office@it-v.net
Phone: +43 6644113324

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KP2XSCMAYZ3NMZA34Z498EMX

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

P10107-40209120074394025
P10107-41409120074394148
P10107-41609120074394162
P10107-41509120074394155
P10107-41909120074394193