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 to rod connector — 11 UDI-DI variants, MDR

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 31, 2026

Spine MUST rod to rod connector

764014274VIS0014R061VX

11 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?

UDI-DI variants

11 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

basicUdiUlid01KSQ0J0GJ1B7S0YNNJJY9QFYR

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

03.56.30007630030861536
03.56.30507630030861574
03.56.30607630030861581
03.56.30207630030861550
03.56.30307630030861567
03.56.30107630030861543
03.56.20007630030861505
03.56.20507630030861512
03.56.20607630030861529
03.56.31007630030861604
03.56.30707630030861598

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 764014274VIS0014R061VX
Device name: —
Device model: Spine MUST rod to rod connector
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