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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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OTOPLAN — 4 UDI-DI variants, MDR (CASCINATION AG)

MD Atlas
CASCINATION AG

Data from EUDAMED, last updated May 23, 2026

OTOPLAN

764016722300OPL001Z7

4 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: CASCINATION AG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 764016722300OPL001Z7
Device name: OTOPLAN
Device model: 2.0.0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jun 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: CASCINATION AG
SRN: CH-MF-000009927
Country: Switzerland
Email: info@cascination.com
Phone: +41 31 552 0440

Authorised representative

Name: CAScination Deutschland GmbH
SRN: DE-AR-000008247
Country: Germany
Phone: +493043776555

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FHAADMHRXNY138EBQK9KF592

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

2007207640167220724
2007207616962000205
2007207640167222438
2007207616962000304