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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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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

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UDI-DI variants

204 UDI-DI variants

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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 ALIF10705034555331
CONDUIT ALIF10705034556512
CONDUIT ALIF10705034556437
CONDUIT ALIF10705034555454
CONDUIT ALIF10705034556444
CONDUIT ALIF10705034556406
CONDUIT ALIF10705034555522
CONDUIT ALIF10705034556567
CONDUIT ALIF10705034555621
CONDUIT ALIF10705034555676
CONDUIT ALIF10705034555508
CONDUIT ALIF10705034555423
CONDUIT ALIF10705034555669
CONDUIT ALIF10705034555539
CONDUIT ALIF10705034556390
CONDUIT ALIF10705034555355
CONDUIT ALIF10705034556581
CONDUIT ALIF10705034556352
CONDUIT ALIF10705034556376
CONDUIT ALIF10705034556543
CONDUIT ALIF10705034555591
CONDUIT ALIF10705034556499
CONDUIT ALIF10705034555485
CONDUIT ALIF10705034555515
CONDUIT ALIF10705034555492

1 2 3 4 5

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