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 — 90 UDI-DI variants, MDR (Medos International SARL)

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Conduit Trial

0705034a001996N

90 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: 0705034a001996N
Device name: Conduit Trial
Device model: Conduit Cervical 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

90 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

basicUdiUlid01KABXA14YBBFYK5NGV9MYBHT1

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 Cervical10705034556093
CONDUIT Cervical10705034556055
CONDUIT Cervical10705034558226
CONDUIT Cervical10705034558400
CONDUIT Cervical10705034555850
CONDUIT Cervical10705034556161
CONDUIT Cervical10705034558646
CONDUIT Cervical10705034558479
CONDUIT Cervical10705034558301
CONDUIT Cervical10705034558509
CONDUIT Cervical10705034558233
CONDUIT Cervical10705034555720
CONDUIT Cervical10705034556109
CONDUIT Cervical10705034555935
CONDUIT Cervical10705034555997
CONDUIT Cervical10705034555768
CONDUIT Cervical10705034558431
CONDUIT Cervical10705034558615
CONDUIT Cervical10705034558622
CONDUIT Cervical10705034558592
CONDUIT Cervical10705034555980
CONDUIT Cervical10705034555751
CONDUIT Cervical10705034555775
CONDUIT Cervical10705034558349
CONDUIT Cervical10705034555799

1 2 3 4