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.

Spine MUST rod — 281 UDI-DI variants, MDR (Medacta International SA)

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 31, 2026

Spine MUST rod

764014274VIS0064R061XY

281 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: Medacta International SA

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: 764014274VIS0064R061XY
Device name: —
Device model: Spine MUST rod
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medacta International SA
SRN: CH-MF-000033473
Country: Switzerland
Email: info@medacta.ch
Phone: +41916966060

Authorised representative

Name: Medacta Italia srl
SRN: IT-AR-000022505
Country: Italy

Variants by status

UDI-DI variants

281 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

basicUdiUlid01KSQ0HWRW0QMEHFX3WVDX5X7N

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

03.68.91407630542713071
03.50.40007630030835339
03.50.40107630030835346
03.50.40207630030835353
03.50.40307630030835360
03.50.40407630345708755
03.68.90507630542712982
03.68.90607630542712999
03.68.90707630542713002
03.68.90807630542713019
03.68.90907630542713026
03.50.80007630030861307
03.50.80107630030861314
03.50.80207630030861321
03.50.80307630030861338
03.68.100407630542723230
03.68.100507630542723247
03.68.100607630542723254
03.68.100707630542723261
03.68.100007630542723193
03.68.100107630542723209
03.68.100207630542723216
03.68.100307630542723223
03.68.101207630542723711
03.68.101307630542723728