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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Stainless Steel LCP Medial Proximal… — 28 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Stainless Steel LCP Medial Proximal Tibial Plate 4.5/5.0 Implants

7611819a00305J9

28 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

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UDI-DI variants

28 UDI-DI variants

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basicUdiUlid01K1EEHTZEZV53DB647Y89S31M

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

239.996S07611819917019
239.99107611819916685
239.992S07611819916975
239.98807611819916654
239.98907611819916661
239.997S07611819917026
239.991S07611819916968
239.99007611819916678
239.99507611819916722
239.989S07611819916944
239.995S07611819917002
239.98607611819916630
239.990S07611819916951
239.99207611819916692
239.986S07611819916913
239.984S07611819916890
239.994S07611819916999
239.985S07611819916906
239.987S07611819916920
239.98707611819916647
239.98407611819916616
239.99607611819916739
239.99407611819916715
239.99707611819916746
239.988S07611819916937

1 2

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00305J9
Device name: Stainless Steel LCP Medial Proximal Tibial Plate 4.5/5.0 Implants
Device model: Stainless Steel LCP Medial Proximal Tibial Plate 4.5/5.0 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