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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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Precise — 11 UDI-DI variants, MDR

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data from EUDAMED, last updated May 23, 2026

Precise

42502961531LM

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: 42502961531LM
Device name: Precise
Device model: Precise
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 26, 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

basicUdiUlid01K62HFYKMZZARZCJG4S1T9EMX

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

531.00020.759004250296150408
531.00055.759004250296150422
531.00060.759004250296150385
531.00045.759004250296162623
531.00084.759004250296180337
531.00025.759004250296162630
531.00083.759004250296180351
531.00085.759004250296180344
531.00081.759004250296180320
531.00000.759004250296147439
531.00005.759004250296150378