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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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Graft Preparation Station — 7 UDI-DI variants, MDR

MD Atlas
GETSCH+HILLER Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Graft Preparation Station

4059426PREP4V

7 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

Reusable

Identity & classification

Basic UDI-DI: 4059426PREP4V
Device name: Graft Preparation Station
Device model: Graft Preparation Station
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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNP64QW99X3EY4K2WB0CHR8R

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

44-00-002104059426202860
44-00-002204059426202877
44-00-002604059426202914
44-00-002004059426231549
44-00-0024 04059426202891
44-00-0025 04059426229768
44-00-002304059426202907