gudid
Primary ID: 04P5733
ARCHITECT (UDI 04P5733)
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 04P5733
Device Regulatory Overview
The ARCHITECT (Model/Catalog Number: 04P5733) is a medical device manufactured by ABBOTT LABORATORIES. This product is indexed under FDA Product Code / Category Classification JJE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04P5733
- Product Code / EMDN
- JJE
- Device Name
- ARCHITECT i1000SR System e-Assay CD-ROM-US Version 33.0
- 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 04P5733.
What classification code is assigned to this device?
This device is registered under product classification code JJE.
Similar Classification Devices (JJE)
Other Devices by ABBOTT LABORATORIES
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