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

210204000004504048145192576
049001004004004059465489642
300210000004104059465026090
210501000004104048145044097
210201002004704059465441251
049900004004304059465487754
280354000004504059465303511
300200000004104059465026496
260402001004004059465444948
047402005004004059465457788
047494000003704059465271308
046504001004204059465452165
280374000004504055107494357
260304002004604059465445563
240304006004304059465477519
251152000003704048145385046
220404001004004059465437308
046202000004304059465294338
210901000004704048145862073
047170000003804059465274590
300202000003804059465026540
213704000004204048145394543
250104001003804059465446164
210200000004104048145045674
300100004003904059465466001