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

212831000004504048145034838
210500000004604048145044189
211722000004704059465238509
047411000004304059465270806
280300000004504059465021644
049004001003704059465490570
213394000004204059465237816
047712000004204059465272312
300101004004304059465466124
270210000003704048145846134
300260000004304059465025710
211730000004304059465238783
240302000004004048145014182
221594000003604059465000694
046404006004404059465451861
223602000003804048145389099
047404006004304059465458211
046404006004204059465451847
220440000004304059465229781
280104001004104059465460719
280102008004704059465463413
212631000004404059465003534
224092000004104048145997140
270101002004004059465443620
210202003004704059465441657

1 2 3 4 5