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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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Layer — 52 UDI-DI variants, MDR (ulrich GmbH & Co. KG)

MD Atlas
ulrich GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Layer

4052536000226Q8

52 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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UDI-DI variants

52 UDI-DI variants

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Applied filters

basicUdiUlid01JXM8N8D2B41PQMPW3HKN5ST2

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 3890-012-00104052536220311
CS 3890-830-00104052536221042
CS 3890-013-90104052536203468
CS 3890-017-00204052536220472
CS 3890-018-00104052536220502
CS 3890-014-00104052536220359
CS 3890-022-00104052536220571
CS 3890-021-00204052536220564
CS 3890-021-00104052536220557
CS 3890-015-00104052536220380
CS 3890-010-00104052536220212
CS 3890-012-00204052536220328
CS 3890-010-00204052536220229
CS 3890-014-00204052536220366
CS 3890-031-00104052536220670
CS 3890-017-70104052536203161
CS 3890-011-00204052536220304
CS 3890-019-00204052536203260
CS 3890-016-00204052536220410
CS 3890-017-00304052536220489
CS 3890-018-80104052536203208
CS 3890-012-30204052536203147
CS 3890-011-00104052536220298
CS 3890-023-00204052536203239
CS 3890-019-00104052536203253

1 2 3

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4052536000226Q8
Device name: —
Device model: Layer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 13, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status