gudid
Primary ID: 1.29.1
Preview (UDI 1.29.1)
Manufactured by Genesis Software Innovations LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Preview - Primary ID 1.29.1
Device Regulatory Overview
The Preview (Model/Catalog Number: 1.29.1) is a medical device manufactured by Genesis Software Innovations LLC. This product is indexed under FDA Product Code / Category Classification QIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.29.1
- Product Code / EMDN
- QIH
- Device Name
- The Preview Shoulder, a 3D total shoulder arthroplasty (TSA) surgical planning software, is a standalone software application which assists the surgeon in planning reverse and anatomic shoulder arthroplasty. Preview Shoulder includes 3D digital representations of implants for placement in images used for surgical planning. Preview Shoulder is a secure software application used by qualified or trained surgeons and is accessed by authorized users. The primary function of Preview Shoulder is to receive and process DICOM CT image(s) of patients. Preview Shoulder can be used to place an implant in the original CT image and place an implant in the 3D model of reconstructed bone. The Preview Shoulder allow the user to perform surgical planning and generate an output surgical report. Preview Shoulder does not provide a diagnosis or surgical recommendation. The surgeon is responsible for selecting and placing the implant model for pre-surgical planning purposes.
- Database Sync Date
- 2026-08-09 09:06:20
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Preview?
The registered manufacturer of record for Preview is Genesis Software Innovations LLC.
What is the Primary UDI-DI identifier for Preview?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.29.1.
What classification code is assigned to this device?
This device is registered under product classification code QIH.
Similar Classification Devices (QIH)
Other Devices by Genesis Software Innovations LLC
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