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.

End to End Dual Connector, Fixed… — 245 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

End to End Dual Connector, Fixed Lateral Connector, Open/Closed Connector, SFX Cross Connector, Side by Side Dual Connector

0705034a001596A

245 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: Medos International SARL

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: 0705034a001596A
Device name: End to End Dual Connector, Fixed Lateral Connector, Open/Closed Connector, SFX Cross Connector, Side by Side Dual Connector
Device model: EXPEDIUM Spine System Connector
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medos International SARL
SRN: CH-MF-000014268
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 32 934 80 00

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

245 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

basicUdiUlid01KM0WRT7CC6NYEBA80YH0HEBW

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

EXPEDIUM SPINE SYSTEM10705034031903
EXPEDIUM SPINE SYSTEM10705034082769
EXPEDIUM SPINE SYSTEM10705034385372
EXPEDIUM SPINE SYSTEM10705034406176
EXPEDIUM SPINE SYSTEM10705034078250
EXPEDIUM SPINE SYSTEM10705034251721
EXPEDIUM SPINE SYSTEM10705034384887
EXPEDIUM SPINE SYSTEM10705034108971
EXPEDIUM SPINE SYSTEM10705034178646
EXPEDIUM SPINE SYSTEM10705034093970
EXPEDIUM SPINE SYSTEM10705034094120
EXPEDIUM SPINE SYSTEM10705034251707
EXPEDIUM SPINE SYSTEM10705034091914
MONARCH SPINE SYSTEM10705034061863
MONARCH SPINE SYSTEM10705034063058
MONARCH SPINE SYSTEM10705034063027
MONARCH SPINE SYSTEM10705034061856
MONARCH SPINE SYSTEM10705034061887
MONARCH SPINE SYSTEM10705034061870
MONARCH SPINE SYSTEM10705034063010