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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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ALM Tube I.D. 6.0, O.D. 8.2 — 4 UDI-DI variants, MDR

MD Atlas
inomed Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

ALM Tube I.D. 6.0, O.D. 8.2

42503076IZE0709B

4 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: inomed Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503076IZE0709B
Device name: ALM Tube I.D. 6.0, O.D. 8.2
Device model: 520843
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: inomed Medizintechnik GmbH
SRN: DE-MF-000005589
Country: Germany
Email: info@inomed.com
Phone: +49764194140

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KMQES8AVXHQXPB4HH891GF29

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

ALM Tube I.D. 7.5, O.D. 10.304250307611362
ALM Tube I.D. 8.0, O.D. 11.004250307611355
ALM Tube, I.D. 7.0, O.D. 9.704250307611379
ALM Tube, ID 6.0, OD 8.204250307611911