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.

Matrix Pedicle Screw Polyaxial… — 582 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Matrix Pedicle Screw Polyaxial Cannulated Reduction Screw

7611819a00266JQ

582 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: 7611819a00266JQ
Device name: Matrix Pedicle Screw Polyaxial Cannulated Reduction Screw
Device model: Matrix Spine Bone Screw
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 8, 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

582 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

basicUdiUlid01K25JEHZM7Y9QRFTE2NCDKPF1

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

04.616.945S07611819366862
04.634.52007611819344990
04.616.750S07611819366701
04.639.899S07611819471382
04.606.760S07611819479487
04.606.740S07611819479449
04.606.650S07611819479371
04.632.970S07611819366022
04.606.750S07611819479463
04.606.65507611819343795
04.639.94507611819378872
04.632.725S07611819365667
04.639.97007611819378926
04.639.42007611819378292
04.634.86007611819345331
04.632.975S07611819366039
04.606.765S07611819479494
04.639.980S07611819471498
04.632.120S07611819365308
04.632.42807611819347557
04.606.96507611819344075
04.634.73507611819345195
04.606.625S07611819479326
04.606.735S07611819479432
04.639.660S07611819471092