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

04.634.85007611819345317
04.639.43807611819378353
04.632.89907611819348073
04.632.999S07611819366060
04.634.54507611819345041
04.632.12007611819347441
04.606.63007611819343740
04.632.945S07611819365971
04.639.750S07611819471160
04.632.990S07611819366053
04.616.85007611819343542
04.616.865S07611819366824
04.634.76507611819345256
04.634.550S07611819368644
04.606.665S07611819479401
04.632.520S07611819365483
04.616.84007611819343528
04.606.525S07611819476547
04.634.440S07611819368569
04.634.825S07611819368859
04.634.665S07611819368750
04.632.790S07611819365780
04.606.86507611819343993
04.634.735S07611819368781
04.639.66007611819378544