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

240304001004204059465473146
280001003004204059465459287
210281000004004059465234594
300211000004104059465026250
049312001004204059465498941
222711000003904059465299814
213404000004104048145379304
221592000003904059465000564
280422000004404059465023242
300101001003704059465465103
047481000004304059465295533
274252000004204059465011478
212021000004104059465295076
046490000004504059465280621
047770000004304059465271841
049310004003804059465497708
049322003003904059465488997
213651000004504048145380225
212702000004204048145036542
210539000004804059465470879
048221001004004059465495421
300152000004004055107360430
251154000003604048145385114
048201001004404059465483480
240301003004604059465474204