gudid
Primary ID: CD3A
CD3A (UDI CD3A)
Manufactured by Aei Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CD3A - Primary ID CD3A
Device Regulatory Overview
The CD3A (Model/Catalog Number: CD3A) is a medical device manufactured by Aei Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification CCK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CD3A
- Product Code / EMDN
- CCK
- Device Name
- Carbon Dioxide Analyzer
- Database Sync Date
- 2026-08-09 09:06:20
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 CD3A?
The registered manufacturer of record for CD3A is Aei Technologies, Inc..
What is the Primary UDI-DI identifier for CD3A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CD3A.
What classification code is assigned to this device?
This device is registered under product classification code CCK.
Similar Classification Devices (CCK)
Other Devices by Aei Technologies, Inc.
Programmatic Export
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