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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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2080456K19P030 — 6 UDI-DI variants, MDR (Drägerwerk AG & Co. KGaA)

MD Atlas
Drägerwerk AG & Co. KGaA

Data from EUDAMED, last updated May 31, 2026

2080456K19P030

0404867512080456K19P030T4

6 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: Drägerwerk AG & Co. KGaA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0404867512080456K19P030T4
Device name: —
Device model: 2080456K19P030
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KSMXG2W67K76X2DH4ZMGA11S

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

Anest. ID Set Coax WT GSL 21004048675637233
Anesth Set Coax WT 210 (BagCone OD22)04048675716082
Anesth Set Coax WT GSL 210(BagCone OD22)04048675716129
VentStar Anesth WT (P) 180 oLL (BC OD22)04048675716006
VentStar Anesth WT (P)180 (BC OD22)04048675715986
VentStar Anesth WT 280 (BagCone OD22)04048675716044