Fully Automatic Urine Sediment Analyzer (UDI 06975488440584)
Manufactured by Infitek Co., Ltd.
Device Regulatory Overview
The Fully Automatic Urine Sediment Analyzer (Model/Catalog Number: UA-S3-120) is a medical device manufactured by Infitek Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0201010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UA-S3-120
- Product Code / EMDN
- W0201010202
- Device Name
- Urine Sediment Analyzer
- Database Sync Date
- 2026-08-09 18:36:58
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 Fully Automatic Urine Sediment Analyzer?
The registered manufacturer of record for Fully Automatic Urine Sediment Analyzer is Infitek Co., Ltd..
What is the Primary UDI-DI identifier for Fully Automatic Urine Sediment Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975488440584.
What classification code is assigned to this device?
This device is registered under product classification code W0201010202.
Similar Classification Devices (W0201010202)
Other Devices by Infitek Co., Ltd.
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