gudid
Primary ID: 04T0320
ARCHITECT (UDI 04T0320)
Manufactured by ABBOTT IRELAND
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARCHITECT - Primary ID 04T0320
Device Regulatory Overview
The ARCHITECT (Model/Catalog Number: 04T0320) is a medical device manufactured by ABBOTT IRELAND. This product is indexed under FDA Product Code / Category Classification CFJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04T0320
- Product Code / EMDN
- CFJ
- Device Name
- Lactate Dehydrogenase2
- Database Sync Date
- 2026-08-09 10:02:49
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 ARCHITECT?
The registered manufacturer of record for ARCHITECT is ABBOTT IRELAND.
What is the Primary UDI-DI identifier for ARCHITECT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04T0320.
What classification code is assigned to this device?
This device is registered under product classification code CFJ.
Similar Classification Devices (CFJ)
Other Devices by ABBOTT IRELAND
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