AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 ST (UDI 04560189284616)
Manufactured by Tosoh Corporation
Device Regulatory Overview
The AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 ST (Model/Catalog Number: 0022100) is a medical device manufactured by Tosoh Corporation. This product is indexed under FDA Product Code / Category Classification W0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0022100
- Product Code / EMDN
- W0201020102
- Device Name
- AUTOMATED ENZYME IMMUNOASSAY SYSTEM AIA-360
- Database Sync Date
- 2026-08-09 17:56:48
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 AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 ST?
The registered manufacturer of record for AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 ST is Tosoh Corporation.
What is the Primary UDI-DI identifier for AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 ST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560189284616.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by Tosoh Corporation
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