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 Spine Instruments for Insertion… — 72 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Matrix Spine Instruments for Insertion and Extraction

7611819a00126J7

72 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

Reusable

Identity & classification

Basic UDI-DI: 7611819a00126J7
Device name: Matrix Spine Instruments for Insertion and Extraction
Device model: Matrix Spine Instruments for Insertion and Extraction
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 14, 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

72 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

basicUdiUlid01K058215PCX4PGH0CXHF4JZE6

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

03.632.20407611819377479
03.616.04407611819417410
03.632.06007611819379596
03.632.02007611819379336
03.632.00607611819378094
03.616.06307611819417595
03.616.05707611819417533
03.616.04207611819416895
03.632.07207611819379602
03.632.01007611819379237
03.632.07407611819377301
03.637.00107611819433830
03.632.40907611819519114
03.632.07507611819377318
03.632.04207611819387973
03.632.02507611819379381
03.632.00307611819391468
03.632.00707611819379206
03.632.01107611819379244
03.632.00107611819378056
03.616.04007611819416871
03.616.05207611819417489
03.632.40107611819502031
03.632.05807611819379589
03.632.03707611819379442

1 2 3