gudid
Primary ID: 3P39-21
ARCHITECT (UDI 3P39-21)
Manufactured by ABBOTT LABORATORIES
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARCHITECT - Primary ID 3P39-21
Device Regulatory Overview
The ARCHITECT (Model/Catalog Number: 3P39-21) is a medical device manufactured by ABBOTT LABORATORIES. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3P39-21
- Product Code / EMDN
- KNK
- Device Name
- Uric Acid
- 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 LABORATORIES.
What is the Primary UDI-DI identifier for ARCHITECT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3P39-21.
What classification code is assigned to this device?
This device is registered under product classification code KNK.
Similar Classification Devices (KNK)
Other Devices by ABBOTT LABORATORIES
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