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.

Stainless Steel LCP Proximal Tibial… — 56 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Stainless Steel LCP Proximal Tibial Plate 3.5 Implants

7611819a00309JH

56 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: 7611819a00309JH
Device name: Stainless Steel LCP Proximal Tibial Plate 3.5 Implants
Device model: Stainless Steel LCP Proximal Tibial Plate 3.5 Implants - Plates
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 30, 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

56 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

basicUdiUlid01K1EEHJXTZQ204JT0E5M2H556

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

239.93507611819800571
239.944S07611819807716
239.942S07611819807693
239.94107611819800632
02.124.216S07611819458505
02.124.213S07611819458192
239.943S07611819807709
02.124.217S07611819458512
02.124.212S07611819458185
239.94207611819800649
02.124.20507611819420304
02.124.22007611819420373
239.93807611819800601
02.124.20407611819418899
239.945S07611819807723
239.937S07611819807648
02.124.21607611819420359
02.124.21707611819420366
02.124.20907611819420328
02.124.22107611819420380
239.94407611819800663
02.124.209S07611819458727
02.124.208S07611819458161
239.93407611819800564
02.124.22507611819420403

1 2 3