MUSE (UDI NX R2)
Manufactured by Ge Medical Systems Information Technologies, Inc.
Device Regulatory Overview
The MUSE (Model/Catalog Number: NX R2) is a medical device manufactured by Ge Medical Systems Information Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NX R2
- Product Code / EMDN
- DQK
- Device Name
- MUSE NX R2 SOFTWARE
- Database Sync Date
- 2026-08-09 09:14:30
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 MUSE?
The registered manufacturer of record for MUSE is Ge Medical Systems Information Technologies, Inc..
What is the Primary UDI-DI identifier for MUSE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NX R2.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by Ge Medical Systems Information Technologies, Inc.
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