gudid
Primary ID: Pro
NeuroLF (UDI Pro)
Manufactured by Positrigo AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeuroLF - Primary ID Pro
Device Regulatory Overview
The NeuroLF (Model/Catalog Number: Pro) is a medical device manufactured by Positrigo AG. This product is indexed under FDA Product Code / Category Classification KPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Pro
- Product Code / EMDN
- KPS
- Device Name
- The NeuroLF is a small aperture Positron Emission Tomography (PET) scanner that produces images of the distribution of positron-emitting isotopes from parts of a subject that are put into the aperture for medical diagnostic and research purposes.
- Database Sync Date
- 2026-08-09 09:00:28
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 NeuroLF?
The registered manufacturer of record for NeuroLF is Positrigo AG.
What is the Primary UDI-DI identifier for NeuroLF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Pro.
What classification code is assigned to this device?
This device is registered under product classification code KPS.
Similar Classification Devices (KPS)
Other Devices by Positrigo AG
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