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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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1080106K19L020 — 2 UDI-DI variants, MDR (Drägerwerk AG & Co. KGaA)

MD Atlas
Drägerwerk AG & Co. KGaA

Data from EUDAMED, last updated May 31, 2026

1080106K19L020

0404867511080106K19L020JG

2 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: Drägerwerk AG & Co. KGaA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0404867511080106K19L020JG
Device name: —
Device model: 1080106K19L020
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Drägerwerk AG & Co. KGaA
SRN: DE-MF-000005329
Country: Germany
Email: EUDAMED@draeger.com
Phone: +49 451 882 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSMP5E3HY5GJM29SVEB73P2F

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

Headgear disp.,soft rub.,large04048675041078
Headgear disp.,soft rub.,small04048675041061