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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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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

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UDI-DI variants

582 UDI-DI variants

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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

04.616.66507611819343399
04.632.545S07611819365537
04.639.155S07611819470828
04.616.55007611819339095
04.616.735S07611819366671
04.606.860S07611819479579
04.632.44007611819347601
04.632.750S07611819365711
04.632.435S07611819365445
04.606.52507611819343665
04.634.150S07611819368491
04.632.96007611819348141
04.639.78007611819378674
04.632.15007611819347502
04.634.535S07611819368613
04.632.76007611819347878
04.632.43507611819347588
04.606.755S07611819479470
04.632.655S07611819365636
04.639.15507611819429840
04.632.155S07611819365377
04.632.135S07611819365339
04.616.62007611819389960
04.632.94507611819348110
04.616.74007611819343436

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