gudid
Primary ID: 07P9001
Alinity (UDI 07P9001)
Manufactured by Abbott Ireland Diagnostics
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alinity - Primary ID 07P9001
Device Regulatory Overview
The Alinity (Model/Catalog Number: 07P9001) is a medical device manufactured by Abbott Ireland Diagnostics. This product is indexed under FDA Product Code / Category Classification LOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07P9001
- Product Code / EMDN
- LOK
- Device Name
- Alinity i AFP Calibrators
- 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 Diagnostics.
What is the Primary UDI-DI identifier for Alinity?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07P9001.
What classification code is assigned to this device?
This device is registered under product classification code LOK.
Similar Classification Devices (LOK)
Other Devices by Abbott Ireland Diagnostics
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