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.

Conduit Trial — 204 UDI-DI variants, MDR (Medos International SARL)

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Conduit Trial

0705034a002005E

204 UDI-DI variants

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

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

Reusable

Identity & classification

Basic UDI-DI: 0705034a002005E
Device name: Conduit Trial
Device model: Conduit Lumbar Trials
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2025

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

204 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

basicUdiUlid01KABXA14YEMYENR4WK8FPHAHW

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

CONDUIT Straight TLIF / PLIF10705034557182
CONDUIT Straight TLIF / PLIF10705034557298
CONDUIT Straight TLIF / PLIF10705034558066
CONDUIT Straight TLIF / PLIF10705034557236
CONDUIT Straight TLIF / PLIF10705034557304
CONDUIT Straight TLIF / PLIF10705034557175
CONDUIT Straight TLIF / PLIF10705034557281
CONDUIT Straight TLIF / PLIF10705034557267
CONDUIT Straight TLIF / PLIF10705034557229
CONDUIT Straight TLIF / PLIF10705034557199
CONDUIT Straight TLIF / PLIF10705034557212
CONDUIT Straight TLIF / PLIF10705034558035
CONDUIT Straight TLIF / PLIF10705034557342
CONDUIT Straight TLIF / PLIF10705034557328
CONDUIT Straight TLIF / PLIF10705034557359
CONDUIT Straight TLIF / PLIF10705034557250
CONDUIT Straight TLIF / PLIF10705034557991
CONDUIT Straight TLIF / PLIF10705034558004
CONDUIT Straight TLIF / PLIF10705034557373
CONDUIT Straight TLIF / PLIF10705034557335
CONDUIT Straight TLIF / PLIF10705034558011
CONDUIT Straight TLIF / PLIF10705034557984
CONDUIT Straight TLIF / PLIF10705034557243
CONDUIT Straight TLIF / PLIF10705034557311
CONDUIT Straight TLIF / PLIF10705034557205

5 6 7 8 9