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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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MatrixNEURO Plates, Mesh Plates and… — 144 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

MatrixNEURO Plates, Mesh Plates and Burr Hole Covers

7611819a00674KB

144 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

144 UDI-DI variants

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basicUdiUlid01K31R085QFYEWNZQKNSPPVSBE

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

04.503.092S07611819916548
04.503.149S07611819609457
04.503.09407611819916579
04.503.071S07611819901223
04.503.090S07611819916500
04.502.022S07611819619692
04.503.067S07611819901148
04.503.08607611819916418
04.503.09807611819901452
04.503.082S07611819901346
04.503.06907611819901179
04.503.05707611819900998
04.503.08407611819901377
04.503.029S07611819900967
04.503.12007611819300323
04.503.09307611819916555
04.503.155S07611819674189
04.503.14707611819609495
04.503.06507611819901094
04.503.152S07611819674172
04.503.098S07611819901469
04.502.06207611819608269
04.503.09507611819916593
04.503.070S07611819901209
04.502.073S07611819619883

1 2 3 4 5

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00674KB
Device name: MatrixNEURO Plates, Mesh Plates and Burr Hole Covers
Device model: MatrixNEURO Plates, Mesh Plates and Burr Hole Covers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 19, 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