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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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FinnComfort — 54,397 UDI-DI variants, MDR (Waldi Schuhfabrik GmbH)

MD Atlas
Waldi Schuhfabrik GmbH

Data from EUDAMED, last updated May 23, 2026

FinnComfort

4030457-FinnCo-001-MN

54,397 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: Waldi Schuhfabrik GmbH

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UDI-DI variants

54,397 UDI-DI variants

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Applied filters

basicUdiUlid01KR3AHVVTKD99Q52VK8V9XTW7

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

02501-80005704030457032695
96524-41934500888281382837
02780-90240000691812992319
01165-06017300884906020382
02973-02209900888281093320
05070-90289704030457095195
02557-59548104030457025826
02851-00734500691812303610
02959-90287504030457044889
02058-42721000691812713525
02106-59548100691812790083
02627-60424104030457100509
02562-00100000691812579251
02913-37343600691812833490
82562-39008700691812321171
02989-85039304030457481097
03609-80349704030457511558
01701-90311904030457443286
03436-82806604030457123744
82568-00748400691812897560
83651-84403804030457496770
02399-42712404030457100967
02555-82508104030457097526
02964-90298704030457490839
02282-00737100691812809624

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4030457-FinnCo-001-MN
Device name: FinnComfort
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Waldi Schuhfabrik GmbH
SRN: DE-MF-000016907
Country: Germany
Email: info@finncomfort.de
Phone: +49952192330

Variants by status