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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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Galvanoprodukte — 8 UDI-DI variants, MDR (C.HAFNER GmbH + Co. KG)

MD Atlas
C.HAFNER GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Galvanoprodukte

425193650000000002X5

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: C.HAFNER GmbH + Co. KG

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 425193650000000002X5
Device name: Galvanoprodukte
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: C.HAFNER GmbH + Co. KG
SRN: DE-MF-000006304
Country: Germany
Email: info@c-hafner.de
Phone: +49 7044 90333 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GZG8FFMTDM1FS6CAEWECRN42

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

852104251936500904
852204251936500911
852304251936500928
853904251936500942
854004251936500959
852404251936500935
783704251936500881
783604251936500874