Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

LucRo — 18,698 UDI-DI variants, MDR (Schein Orthopädie Service KG)

MD Atlas
Schein Orthopädie Service KG

Data from EUDAMED, last updated May 23, 2026

LucRo

4055107LucRo7D

18,698 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: Schein Orthopädie Service KG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4055107LucRo7D
Device name: LucRo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Schein Orthopädie Service KG
SRN: DE-MF-000004958
Country: Germany
Email: remscheid@schein.de
Phone: +4921919100

Variants by status

UDI-DI variants

18,698 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KRBAHFPTH32N78MG1EKS4H0T

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

047400005003604059465457580
250302001004004059465481967
250304004004104059465480939
220454000004104048145192989
223252000004304048145022781
260402000003804048145856737
280101004004404059465461921
280234000004604059465254561
280422000004504059465023259
250304000003804048145002684
212841000004204059465236215
220601001003904059465434338
250300005004104059465480618
270182000003804048145845342
223050000004304048145024327
212840000004404059465236079
250202004004104059465474495
213730000004204048145838153
210301000003704048145045018
240231000004004048145012898
240302000003904048145014175
210961000004104048145042925
221591000003804059465000472
047000001004004059465453223
240630000004104048145021029