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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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Metafer — 2 UDI-DI variants, IVDR (MetaSystems Hard & Software GmbH)

MD Atlas
MetaSystems Hard & Software GmbH

Data from EUDAMED, last updated May 23, 2026

Metafer

42504064METAFERF5

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: MetaSystems Hard & Software GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504064METAFERF5
Device name: Metafer
Device model: 4.4
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Special device type: refdata.special-ivd-device-type.software
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: MetaSystems Hard & Software GmbH
SRN: DE-MF-000016548
Country: Germany
Email: info@metasystems-international.com
Phone: +49 6205 39610

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQCJGRHP0YNZD30T3D7N4G9M

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

Metafer04250406460007
Metafer04250406460014