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 Anterior Instruments Guide… — 19 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Expedium Anterior Instruments Guide Holder Impactor Distractor Driver Shaft Wrench

0705034a001205F

19 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: 0705034a001205F
Device name: Expedium Anterior Instruments Guide Holder Impactor Distractor Driver Shaft Wrench
Device model: Expedium Anterior Instruments for Insertion and Extraction of Osteosynthesis Devices
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

19 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

basicUdiUlid01K2QETJXF08E2FWKVHVZ7XRNY

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 ANTERIOR SPINE SYSTEM10705034219462
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219516
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219424
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219295
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219493
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219455
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219318
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219523
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219509
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219271
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219431
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219288
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219332
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219448
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219554
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219301
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219608
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219486
EXPEDIUM ANTERIOR SPINE SYSTEM10705034219325