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.

MatrixORTHOGNATHIC LOCK Screw — 92 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

MatrixORTHOGNATHIC LOCK Screw

7611819a00651JX

92 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: 7611819a00651JX
Device name: MatrixORTHOGNATHIC LOCK Screw
Device model: MatrixORTHOGNATHIC LOCK Screw
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 3, 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

92 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

basicUdiUlid01K95QD0DKK4075AQDBK436VFP

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

04.511.616.01C07611819383852
04.511.642.01C07611819383920
04.511.664.04S07611819386587
04.511.608.04C07611819384033
04.511.640.01S07611819386167
04.511.648.01C07611819383951
04.511.664.01C07611819384200
04.511.614.01S07611819386099
04.511.628.01S07611819384699
04.511.624.04S07611819386549
04.511.638.01C07611819383906
04.511.666.04C07611819384309
04.511.612.01S07611819386082
04.511.618.01C07611819383869
04.511.605.01C07611819383791
04.511.636.04S07611819386372
04.511.666.01S07611819386525
04.511.624.01S07611819384668
04.511.625.01S07611819384675
04.511.644.01S07611819386181
04.511.665.01S07611819386518
04.511.614.01C07611819383845
04.511.618.01S07611819386112
04.511.635.04S07611819386365
04.511.646.01S07611819386198

1 2 3 4