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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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Tray — 13 UDI-DI variants, MDR (ulrich GmbH & Co. KG)

MD Atlas
ulrich GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Tray

4052536000265QJ

13 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: ulrich GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4052536000265QJ
Device name: —
Device model: Tray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: ulrich GmbH & Co. KG
SRN: DE-MF-000006411
Country: Germany
Email: info@ulrichmedical.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01JXJ677SG740D30337KJY7HVK

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

CS 7040-4004052536221226
CS 3890-013-00304052536220342
CS 3890-014-00304052536220373
CS 3890-020-00404052536220540
CS 3890-001-00204052536220113
CS 7040-404052536221219
CS 3890-032-00304052536220762
CS 3890-012-30404052536203628
CS 3890-022-00304052536220595
CS 3872-0304052536220090
CS 3890-016-00704052536220458
CS 3890-017-00404052536220496
CS 3890-015-00204052536220397