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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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301007VK19Z000 — 4 UDI-DI variants, MDR (Drägerwerk AG & Co. KGaA)

MD Atlas
Drägerwerk AG & Co. KGaA

Data from EUDAMED, last updated May 30, 2026

301007VK19Z000

040486751301007VK19Z0006K

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Drägerwerk AG & Co. KGaA

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 040486751301007VK19Z0006K
Device name: —
Device model: 301007VK19Z000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSMSC2S8069MT6MT699ESA48

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

Scio Four04048675429333
Scio Four, Oxi04048675429326
Scio Four, Oxi plus04048675429302
Scio Four, plus04048675429319