gudid
Primary ID: CS200
ClearScan (UDI CS200)
Manufactured by ESI CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearScan - Primary ID CS200
Device Regulatory Overview
The ClearScan (Model/Catalog Number: CS200) is a medical device manufactured by ESI CORPORATION. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CS200
- Product Code / EMDN
- ITX
- Device Name
- ClearScan
- Database Sync Date
- 2026-08-09 09:18:01
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 ClearScan?
The registered manufacturer of record for ClearScan is ESI CORPORATION.
What is the Primary UDI-DI identifier for ClearScan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CS200.
What classification code is assigned to this device?
This device is registered under product classification code ITX.
Similar Classification Devices (ITX)
Other Devices by ESI CORPORATION
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