gudid
Primary ID: 91210
Standard Imaging Lucy 3D QA Phantom (UDI 91210)
Manufactured by STANDARD IMAGING INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Standard Imaging Lucy 3D QA Phantom - Primary ID 91210
Device Regulatory Overview
The Standard Imaging Lucy 3D QA Phantom (Model/Catalog Number: 91210) is a medical device manufactured by STANDARD IMAGING INC.. This product is indexed under FDA Product Code / Category Classification IXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 91210
- Product Code / EMDN
- IXG
- Device Name
- Standard Imaging Lucy 3D QA Phantom is designed to perform comprehensive quality assurance tests for an entire stereotactic radiosurgery/SRT procedure. The phantom allows verification of treatment planning software calculations for volume measurements, distance measurements, image fusion and image transfer. Dosimetry verification is accomplished via components that accommodate ion chambers, film, MOSFETs, TLDs and polymer gels.
- Database Sync Date
- 2026-08-09 09:37:45
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 Standard Imaging Lucy 3D QA Phantom?
The registered manufacturer of record for Standard Imaging Lucy 3D QA Phantom is STANDARD IMAGING INC..
What is the Primary UDI-DI identifier for Standard Imaging Lucy 3D QA Phantom?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 91210.
What classification code is assigned to this device?
This device is registered under product classification code IXG.
Similar Classification Devices (IXG)
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