gudid
Primary ID: 100-1023-100
QUASAR (UDI 100-1023-100)
Manufactured by Modus Medical Devices Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QUASAR - Primary ID 100-1023-100
Device Regulatory Overview
The QUASAR (Model/Catalog Number: 100-1023-100) is a medical device manufactured by Modus Medical Devices Inc. This product is indexed under FDA Product Code / Category Classification LHO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100-1023-100
- Product Code / EMDN
- LHO
- Device Name
- QUASAR MRgRT Insight (MRDQA) Phantom - Support Base Package. Includes Support base and upright sections with 1 laser alignment target, Users Guide, Heavy Duty Case, and software for 1 MR scanner with unlimited scans.
- Database Sync Date
- 2026-08-09 09:03:53
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 QUASAR?
The registered manufacturer of record for QUASAR is Modus Medical Devices Inc.
What is the Primary UDI-DI identifier for QUASAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100-1023-100.
What classification code is assigned to this device?
This device is registered under product classification code LHO.
Similar Classification Devices (LHO)
Other Devices by Modus Medical Devices Inc
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