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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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exoplan — 2 UDI-DI variants, MDR (exocad GmbH)

MD Atlas
exocad GmbH

Data from EUDAMED, last updated May 23, 2026

exoplan

426052136EXOPLAN21A6

2 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: exocad GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426052136EXOPLAN21A6
Device name: exoplan
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: exocad GmbH
SRN: DE-MF-000007341
Country: Germany
Email: info@exocad.com
Phone: +49 6151 629489 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G0EFPAJSEBKZ6KYKQYN8C5FD

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

exoplan 3.0 Galway04260521365019
exoplan 3.1 Rijeka04260521365026