gudid
Primary ID: 7K65-39
ARCHITECT (UDI 7K65-39)
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 7K65-39
Device Regulatory Overview
The ARCHITECT (Model/Catalog Number: 7K65-39) is a medical device manufactured by ABBOTT IRELAND. This product is indexed under FDA Product Code / Category Classification CEC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7K65-39
- Product Code / EMDN
- CEC
- Device Name
- ARCHITECT Free T4 Reagent Kit (500T)
- 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 7K65-39.
What classification code is assigned to this device?
This device is registered under product classification code CEC.
Similar Classification Devices (CEC)
Other Devices by ABBOTT IRELAND
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