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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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Crosslink, sterile, rod to rod — 6 UDI-DI variants, MDR

MD Atlas
ulrich GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Crosslink, sterile, rod to rod

4052536000123PV

6 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: ulrich GmbH & Co. KG

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 4052536000123PV
Device name: —
Device model: Crosslink, sterile, rod to rod
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 11, 2024

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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JCDXX98CXN6SS83N1F543VV1

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 3917-05-S04052536210367
CS 3917-22-S04052536210480
CS 3917-21-S04052536210473
CS 3917-07-S04052536210381
CS 3917-06-S04052536210374
CS 3917-23-S04052536210497