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

03.68.95807630542719707
03.68.95907630542719714
03.68.96007630542719721
03.68.96107630542719738
03.52.65107630345703163
03.52.65207630345703170
03.52.65307630345703187
03.68.98607630542719974
03.68.98707630542719981
03.68.98807630542719998
03.52.60107630345703132
03.52.60207630345703149
03.52.60307630345703156
03.68.98307630542719943
03.68.98407630542719950
03.68.98507630542719967
03.50.43007630030835414
03.50.43107630030835421
03.50.43207630030835438
03.50.43307630030835445
03.50.43407630345708762
03.68.91007630542713033
03.68.91107630542713040
03.68.91207630542713057
03.68.91307630542713064