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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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UNIC® Reverse Shoulder — 2 UDI-DI variants, MDR (EVOLUTIS)

MD Atlas
EVOLUTIS

Data from EUDAMED, last updated May 19, 2026

UNIC® Reverse Shoulder

376025538P090103RCUFA

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class III

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: EVOLUTIS

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Device characteristics

Implantable

Legacy certificates

Certificate number: 017-00-00-MDR
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ITALCERT SRL (0426)
Validity: Apr 6, 2023 → Apr 5, 2028

Identity & classification

Basic UDI-DI: 376025538P090103RCUFA
Device name: UNIC® Reverse Shoulder
Device model: UNIC® Reverse Shoulder
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Nov 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: EVOLUTIS
SRN: FR-MF-000000492
Country: France
Email: qualite@evolutis-group.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HFVT104YPRK9K8CB19QH4882

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

UNIC®03760255384986
UNIC®03760255384993