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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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Inventarabdeckungen — 10 UDI-DI variants, MDR (Imtegra GmbH & Co KG)

MD Atlas
Imtegra GmbH & Co KG

Data from EUDAMED, last updated May 23, 2026

Inventarabdeckungen

4260253262207SB

10 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: Imtegra GmbH & Co KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260253262207SB
Device name: Inventarabdeckungen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Imtegra GmbH & Co KG
SRN: DE-MF-000006451
Country: Germany
Email: info@imtegra.de
Phone: +493811217210

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJ7CKYR2HNJEYN4PR3SFCEAV

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

2207 500604260530129350
2207 503004260253260743
2207 503204260253260767
2207 500204260253260668
2207 500804260253260682
2207 503304260253260774
2207 500404260253260675
2207 503104260253260750
2207 501404260253260736
2207 500904260253260699