Mission U120 Urine Analyzer (UDI U111-111)
Manufactured by Acon Laboratories, Inc.
Device Regulatory Overview
The Mission U120 Urine Analyzer (Model/Catalog Number: U111-111) is a medical device manufactured by Acon Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification KQO within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- U111-111
- Product Code / EMDN
- KQO
- Device Name
- Mission U120 Urine Analyzer with Barcode Reader
- Database Sync Date
- 2026-08-09 10:01:48
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 Mission U120 Urine Analyzer?
The registered manufacturer of record for Mission U120 Urine Analyzer is Acon Laboratories, Inc..
What is the Primary UDI-DI identifier for Mission U120 Urine Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is U111-111.
What classification code is assigned to this device?
This device is registered under product classification code KQO.
Similar Classification Devices (KQO)
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