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 screw (tulip) — 1,721 UDI-DI variants, MDR

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 31, 2026

Spine MUST screw (tulip)

764014274VIS0084R061YS

1,721 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: 764014274VIS0084R061YS
Device name: —
Device model: Spine MUST screw (tulip)
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

1,721 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

basicUdiUlid01KSQ0J1GVBZ7Q8VDKSAZWV0N0

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

03.58.66307630971296350
03.58.46407630971295063
03.58.26407630971293762
03.58.86407630971297661
03.58.66407630971296367
03.58.46507630971295070
03.58.26507630971293779
03.58.86507630971297678
03.58.66507630971296374
03.58.46607630971295087
03.58.26607630971293786
03.58.86607630971297685
03.58.66607630971296381
03.58.46707630971295094
03.58.26707630971293793
03.58.86707630971297692
03.58.66707630971296398
03.58.46807630971295100
03.58.26807630971293809
03.58.86807630971297708
03.58.66807630971296404
03.58.46907630971295117
03.58.26907630971293816
03.58.86907630971297715
03.58.66907630971296411