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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… — 36 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Stainless Steel LCP Medial Proximal Tibial Plate 3.5 Implants

7611819a00303J5

36 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

36 UDI-DI variants

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basicUdiUlid01K1EEHX2RRDNPT9T6XMYAN3ZM

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

239.95407611819912052
239.96407611819915558
239.95807611819912090
239.954S07611819911703
239.960S07611819915961
239.965S07611819916012
239.96607611819915572
239.96207611819915534
239.968S07611819916043
239.956S07611819915923
239.96007611819915510
239.963S07611819915992
239.966S07611819916029
239.959S07611819915954
239.958S07611819915947
239.962S07611819915985
239.95607611819912076
239.967S07611819916036
239.955S07611819915916
239.97007611819915619
239.96307611819915541
239.969S07611819916050
239.964S07611819916005
239.95907611819912106
239.96707611819915589

1 2

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00303J5
Device name: Stainless Steel LCP Medial Proximal Tibial Plate 3.5 Implants
Device model: Stainless Steel LCP Medial 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