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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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Instrument Disinfectant — 36 UDI-DI variants, MDR

MD Atlas
Laboratorium Dr. Deppe GmbH

Data from EUDAMED, last updated May 30, 2026

Instrument Disinfectant

4260181255126SL

36 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: Laboratorium Dr. Deppe GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260181255126SL
Device name: Instrument Disinfectant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratorium Dr. Deppe GmbH
SRN: DE-MF-000005103
Country: Germany
Email: qm@drdeppe.de
Phone: +49215255650

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHP1N2GD4E794HECZGXFHYP

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

60178604260181257310
60178704260181257303
60172604260181256511
60172704260181256535
60172804260181256559
60020904260181256108
60021004260181256115
60021504260181256139
60021404260181256122
60021304260181256146
60002404260181256153

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