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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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CAS-One IR Software — 3 UDI-DI variants, MDR (CASCINATION AG)

MD Atlas
CASCINATION AG

Data from EUDAMED, last updated May 23, 2026

CAS-One IR Software

764016722300C1R001KB

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: CASCINATION AG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 764016722300C1R001KB
Device name: CAS-One IR Software
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Dec 12, 2025

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KC8PKRKCNJ150Q17F0HRG47Y

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

2001607616962000090
2001607616962000236
2001607616962000281