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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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DracoFoam Infekt Pro — 8 UDI-DI variants, MDR

MD Atlas
Dr. Ausbüttel GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

DracoFoam Infekt Pro

42600558305578

8 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: Dr. Ausbüttel GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42600558305578
Device name: DracoFoam Infekt Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dr. Ausbüttel GmbH & Co. KG
SRN: DE-MF-000005465
Country: Germany
Email: info@drausbuettel.de
Phone: +49 231 28666 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR0TE2ZM30N0M41D7DX103BK

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

1401304262406530727
14013-M204262406530833
1401404262406530734
14014-M204262406530840
1401504262406530741
14015-M204262406530857
1401204262406530703
14012-M204262406530710