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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 setscrew — 12 UDI-DI variants, MDR

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 31, 2026

Spine MUST setscrew

764014274VIS0024R061WC

12 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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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 764014274VIS0024R061WC
Device name: —
Device model: Spine MUST setscrew
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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KSQ0J2HRRDB2CVXQ2PN6ZWJ9

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

03.57.90307630971278974
03.57.90407630971288843
03.57.90507630971288850
03.57.90607630971288867
03.50.20107630040716062
03.50.20207630040716079
03.50.20407630040716086
03.50.20607630040717069
03.50.20807630040717052
03.56.21107630030885433
03.56.21207630030885440
03.50.20007630030834844