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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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Container und Siebkörbe — 55 UDI-DI variants, MDR

MD Atlas
GETSCH+HILLER Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Container und Siebkörbe

4059426CONT2N

55 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: GETSCH+HILLER Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4059426CONT2N
Device name: Container und Siebkörbe
Device model: Container und Siebkörbe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: GETSCH+HILLER Medizintechnik GmbH
SRN: DE-MF-000007007
Country: Germany
Email: info@getsch-hiller.de
Phone: +49 7461 13051-0

Variants by status

UDI-DI variants

55 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNPCFWTDQJT1BN7V5ESBKNVT

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

90-02-103004059426084459
90-10-000104059426105512
90-10-000204059426105628
90-01-104504059426239194
90-01-104504059426193670

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