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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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Finesse² — 11 UDI-DI variants, MDR

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data from EUDAMED, last updated May 23, 2026

Finesse²

42502961535LV

11 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: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502961535LV
Device name: Finesse²
Device model: Finesse²
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft
SRN: DE-MF-000009663
Country: Germany
Email: service@erka.org
Phone: +49 (0) 8041/80090

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01K6CTHJ8T6D43J0P8748X9M10

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

535.00055.759004250296148566
535.00060.759004250296149273
535.00025.759004250296151139
535.00045.759004250296148528
535.00085.759004250296180399
535.00081.759004250296180368
535.00005.759004250296148511
535.00084.759004250296180375
535.00000.759004250296148238
535.00083.759004250296180382
535.00020.759004250296148542