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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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208044PK19T010 — 3 UDI-DI variants, MDR (Drägerwerk AG & Co. KGaA)

MD Atlas
Drägerwerk AG & Co. KGaA

Data from EUDAMED, last updated May 31, 2026

208044PK19T010

040486751208044PK19T0109Z

3 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: 040486751208044PK19T0109Z
Device name: —
Device model: 208044PK19T010
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSMP5J1JABJ6VG4J431TWHFC

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

Breathing bag 1.5 L, silicone04048675023494
Breathing bag 2.3 L, silicone04048675007135
Breathing bag 3.0 L, silicone04048675023456