GUDIDData
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eudamed_udi Primary ID: 03760255384924

UNIC® (UDI 03760255384924)

Manufactured by EVOLUTIS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UNIC® - Primary ID 03760255384924

Device Regulatory Overview

The UNIC® (Model/Catalog Number: E27 201) is a medical device manufactured by EVOLUTIS. This product is indexed under FDA Product Code / Category Classification P09010303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
E27 201
Product Code / EMDN
P09010303
Device Name
UNIC® Reverse Shoulder
Database Sync Date
2026-08-09 17:49:25

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of UNIC®?

The registered manufacturer of record for UNIC® is EVOLUTIS.

What is the Primary UDI-DI identifier for UNIC®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760255384924.

What classification code is assigned to this device?

This device is registered under product classification code P09010303.

Similar Classification Devices (P09010303)

Other Devices by EVOLUTIS

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