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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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Fixierbandage-kohäsiv — 27 UDI-DI variants, MDR (Franz Kalff GmbH)

MD Atlas
Franz Kalff GmbH

Data from EUDAMED, last updated May 23, 2026

Fixierbandage-kohäsiv

4063921CohesiveBandageGH

27 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: Franz Kalff GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4063921CohesiveBandageGH
Device name: Fixierbandage-kohäsiv
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Franz Kalff GmbH
SRN: DE-MF-000005326
Country: Germany
Email: info@franzkalff.de
Phone: +4922516260

Variants by status

UDI-DI variants

27 UDI-DI variants

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Applied filters

basicUdiUlid01J6VCF3BB2S1KKJHTXHKBF7G3

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

No registered UDI-DI variants for this device family.