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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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DS Core Diagnosis — 2 UDI-DI variants, MDR (Zetta25 AG)

MD Atlas
Zetta25 AG

Data from EUDAMED, last updated May 23, 2026

DS Core Diagnosis

426235235-S3809-000-YM

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: Zetta25 AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426235235-S3809-000-YM
Device name: DS Core Diagnosis
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: Dec 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Zetta25 AG
SRN: CH-MF-000022840
Country: Switzerland
Email: contact@dentsplysirona.com

Authorised representative

Name: DS REP B.V.
SRN: NL-AR-000013154
Country: Netherlands
Phone: +31 79 347 1288

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JEE62SMV1CH1B3N7P1SAF08T

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

0426235235160504262352351605
0426235235351704262352353517