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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 lateral connectors — 7 UDI-DI variants, MDR

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 31, 2026

Spine MUST lateral connectors

764014274VIS0054R061XK

7 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: 764014274VIS0054R061XK
Device name: —
Device model: Spine MUST lateral connectors
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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KSQ0HTAR3CB7KQEW0V3ER3RP

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

03.56.10007630030839818
03.56.10107630030839825
03.56.10207630030839832
03.56.10407630345703217
03.56.10507630345703224
03.56.10607630345703231
03.56.10307630345703200