gudid
Primary ID: 90501
Standard Imaging QA BeamChecker Plus (UDI 90501)
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 QA BeamChecker Plus - Primary ID 90501
Device Regulatory Overview
The Standard Imaging QA BeamChecker Plus (Model/Catalog Number: 90501) is a medical device manufactured by STANDARD IMAGING INC.. This product is indexed under FDA Product Code / Category Classification LHO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90501
- Product Code / EMDN
- LHO
- Device Name
- Standard Imaging QA BeamChecker Plus is a reliable and uncomplicated measurement instrument for daily quality assurance testing of linear accelerator, TomoTherapy Hi Art System, or other rotational delivery treatment machine output.
- 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 QA BeamChecker Plus?
The registered manufacturer of record for Standard Imaging QA BeamChecker Plus is STANDARD IMAGING INC..
What is the Primary UDI-DI identifier for Standard Imaging QA BeamChecker Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90501.
What classification code is assigned to this device?
This device is registered under product classification code LHO.
Similar Classification Devices (LHO)
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