gudid
Primary ID: 07P5121
Alinity (UDI 07P5121)
Manufactured by ABBOTT IRELAND
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alinity - Primary ID 07P5121
Device Regulatory Overview
The Alinity (Model/Catalog Number: 07P5121) is a medical device manufactured by ABBOTT IRELAND. This product is indexed under FDA Product Code / Category Classification DHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07P5121
- Product Code / EMDN
- DHA
- Device Name
- Alinity i Total B-hCG Reagent Kit
- 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 Alinity?
The registered manufacturer of record for Alinity is ABBOTT IRELAND.
What is the Primary UDI-DI identifier for Alinity?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07P5121.
What classification code is assigned to this device?
This device is registered under product classification code DHA.
Similar Classification Devices (DHA)
Other Devices by ABBOTT IRELAND
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