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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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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

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UDI-DI variants

1,721 UDI-DI variants

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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

03.52.31507630030857478
03.52.31607630030857485
03.52.32007630030857553
03.52.32107630030857560
03.52.32207630030857577
03.52.32307630030857584
03.52.32407630030857591
03.52.32507630030857607
03.52.32607630030857614
03.52.32707630030857621
03.52.32807630030857638
03.52.33507630030857737
03.52.33607630030857744
03.52.33707630030857751
03.52.33807630030857768
03.52.33907630030857775
03.52.34007630030857782
03.52.34107630030857799
03.52.34207630030857805
03.52.34307630030857812
03.52.34507630030857829
03.52.34707630030857836
03.52.30107630030884382
03.52.30207630030884399
03.52.30307630030884405

2 3 4 5 6

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