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.

LCP Distal Humerus and LCP… — 84 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

LCP Distal Humerus and LCP Extra-articular Distal Humerus Plate Stainless Steel

7611819a00653K3

84 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: Synthes GmbH

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

Implantable

Identity & classification

Basic UDI-DI: 7611819a00653K3
Device name: LCP Distal Humerus and LCP Extra-articular Distal Humerus Plate Stainless Steel
Device model: LCP Distal Humerus and LCP Extra-articular Distal Humerus Plate Stainless Steel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Synthes GmbH
SRN: CH-MF-000013345
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 (0) 61 965 61 11

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

84 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

basicUdiUlid01JZX8EYXH4STF21S8CH4Q3QXD

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

241.276S07611819828230
241.262S07611819828117
241.30207611819161146
241.28507611819161191
241.27807611819161122
241.284S07611819828292
241.27707611819161115
241.283S07611819828285
241.26207611819160965
241.28707611819161214
241.300S07611819828353
241.26307611819160972
241.28907611819161238
241.289S07611819828346
241.28207611819161160
241.28307611819161177
241.269S07611819828186
241.268S07611819828179
241.278S07611819828254
241.265S07611819828148
241.266S07611819828155
241.301S07611819828360
241.275S07611819828223
241.285S07611819828308
241.263S07611819828124

1 2 3 4