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.

Expedium Verse Reusable Instruments… — 22 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Expedium Verse Reusable Instruments for Insertion and Extraction

0705034a001125G

22 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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: 0705034a001125G
Device name: Expedium Verse Reusable Instruments for Insertion and Extraction
Device model: Expedium Verse Reusable Instruments for Insertion and Extraction
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 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

22 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

basicUdiUlid01K2QETDNZ046KVJ06KZ3MBHC9

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 SYSTEM10705034467290
EXPEDIUM SPINE SYSTEM10705034467306
EXPEDIUM SPINE SYSTEM10705034467245
EXPEDIUM SPINE SYSTEM10705034467399
EXPEDIUM SPINE SYSTEM10705034467528
EXPEDIUM SPINE SYSTEM10705034467115
EXPEDIUM SPINE SYSTEM10705034467191
EXPEDIUM SPINE SYSTEM10705034467184
EXPEDIUM VERSE SPINE SYSTEM10705034467405
EXPEDIUM VERSE SPINE SYSTEM10705034467566
EXPEDIUM VERSE SPINE SYSTEM10705034477190
EXPEDIUM VERSE SPINE SYSTEM10705034467559
EXPEDIUM VERSE SPINE SYSTEM10705034467603
EXPEDIUM VERSE SPINE SYSTEM10705034477206
EXPEDIUM VERSE SPINE SYSTEM10705034467429
EXPEDIUM VERSE SPINE SYSTEM10705034467498
EXPEDIUM VERSE SPINE SYSTEM10705034477138
EXPEDIUM VERSE SPINE SYSTEM10705034467634
EXPEDIUM VERSE SPINE SYSTEM10705034467443
EXPEDIUM VERSE SPINE SYSTEM10705034467450
EXPEDIUM VERSE SPINE SYSTEM10705034467474
EXPEDIUM VERSE SPINE SYSTEM10705034467610