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.

Posterior Parallel Connector Extension… — 30 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Posterior Parallel Connector Extension Connector Claw Connector L-Connector T-Connector

7611819a00389K9

30 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: 7611819a00389K9
Device name: Posterior Parallel Connector Extension Connector Claw Connector L-Connector T-Connector
Device model: Posterior Connectors for Spine Connector
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

30 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

basicUdiUlid01K25JEHZKR4TMDVVG4ASM5NFZ

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

04.633.40307611819348387
04.633.404S07611819497443
04.633.400S07611819497405
04.633.403S07611819497436
04.633.40407611819348394
04.633.40107611819348363
04.633.40007611819348356
04.633.401S07611819497412
498.95907611819717886
498.959S07611819955783
498.165S07611819181113
04.300.002S07611819978072
04.300.00207611819869110
04.300.00307611819869127
04.300.000S07611819978058
04.300.003S07611819978089
04.300.00007611819869097
04.633.402S07611819497429
04.633.40207611819348370
498.159S07611819966369
04.633.40507611819348400
498.16207611819717206
498.160S07611819181106
498.16507611819043985
04.300.00107611819869103

1 2