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 Polyaxial Cannulated/Non… — 286 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

EXPEDIUM Verse Polyaxial Cannulated/Non-Cannulated screws

0705034a0017262

286 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: 0705034a0017262
Device name: EXPEDIUM Verse Polyaxial Cannulated/Non-Cannulated screws
Device model: EXPEDIUM Verse System Bone Screw
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 17, 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

286 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

basicUdiUlid01KA9F2NRWB1J7GEZMYGPXFHF0

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 VERSE SPINE SYSTEM10705034444109
EXPEDIUM VERSE SPINE SYSTEM10705034400303
EXPEDIUM VERSE SPINE SYSTEM10705034400143
EXPEDIUM VERSE SPINE SYSTEM10705034399478
EXPEDIUM VERSE SPINE SYSTEM10705034399546
EXPEDIUM VERSE SPINE SYSTEM10705034442358
EXPEDIUM VERSE SPINE SYSTEM10705034444734
EXPEDIUM VERSE SPINE SYSTEM10705034442563
EXPEDIUM VERSE SPINE SYSTEM10705034401201
EXPEDIUM VERSE SPINE SYSTEM10705034444093
EXPEDIUM VERSE SPINE SYSTEM10705034440767
EXPEDIUM VERSE SPINE SYSTEM10705034401850
EXPEDIUM VERSE SPINE SYSTEM10705034442365
EXPEDIUM VERSE SPINE SYSTEM10705034399553
EXPEDIUM VERSE SPINE SYSTEM10705034443607
EXPEDIUM VERSE SPINE SYSTEM10705034444659
EXPEDIUM VERSE SPINE SYSTEM10705034440637
EXPEDIUM VERSE SPINE SYSTEM10705034443881
EXPEDIUM VERSE SPINE SYSTEM10705034440651
EXPEDIUM VERSE SPINE SYSTEM10705034400204
EXPEDIUM VERSE SPINE SYSTEM10705034400914
EXPEDIUM VERSE SPINE SYSTEM10705034444130
EXPEDIUM VERSE SPINE SYSTEM10705034400402
EXPEDIUM VERSE SPINE SYSTEM10705034399140
EXPEDIUM VERSE SPINE SYSTEM10705034442266

5 6 7 8 9