GUDIDData
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eudamed_udi Primary ID: 08051887989867

GENUS (UDI 08051887989867)

Manufactured by Adler Ortho S.p.A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GENUS - Primary ID 08051887989867

Device Regulatory Overview

The GENUS (Model/Catalog Number: 1138276) is a medical device manufactured by Adler Ortho S.p.A. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1138276
Product Code / EMDN
P0909030101
Device Name
GENUS PS CEMENTED FEMORAL COMPONENT SIZE 67 STANDARD RIGHT
Database Sync Date
2026-08-09 16:30:07

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 GENUS?

The registered manufacturer of record for GENUS is Adler Ortho S.p.A.

What is the Primary UDI-DI identifier for GENUS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051887989867.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by Adler Ortho S.p.A

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