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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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Indicator for validation of cleaning… — 4 UDI-DI variants, MDR

MD Atlas
Pereg GmbH

Data from EUDAMED, last updated May 23, 2026

Indicator for validation of cleaning performance

426005266ResidueDetectUU

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Pereg GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426005266ResidueDetectUU
Device name: Indicator for validation of cleaning performance
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Pereg GmbH
SRN: DE-MF-000048645
Country: Germany
Email: info@pereg.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K394FD1BW52DN5C0JM2C78S6

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

67067-1214260052660123
77080-06D14260052660932
77070-06D14260052660291
67070-2014260052660277