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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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Siebkorb für Instrumentenset CS 2.8-3.5 — 1 UDI-DI variant, MDR

MD Atlas
Meditec Source GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Siebkorb für Instrumentenset CS 2.8-3.5

426246385PG279Z

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Meditec Source GmbH & Co. KG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426246385PG279Z
Device name: Siebkorb für Instrumentenset CS 2.8-3.5
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: Meditec Source GmbH & Co. KG
SRN: DE-MF-000006490
Country: Germany
Email: martin.streng@meditec-source.com
Phone: 017610429389

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01J46F8NH8W7HQFSW8RH4H2F63

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

2701-54804262463851667