eudamed_udi
Primary ID: 07649998522045
NeuroLF Seeat (UDI 07649998522045)
Manufactured by Positrigo AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeuroLF Seeat - Primary ID 07649998522045
Device Regulatory Overview
The NeuroLF Seeat (Model/Catalog Number: NLF-3000-0100) is a medical device manufactured by Positrigo AG. This product is indexed under FDA Product Code / Category Classification Z11020480 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NLF-3000-0100
- Product Code / EMDN
- Z11020480
- Device Name
- NeuroLF Seat
- Database Sync Date
- 2026-08-09 18:00:59
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 Seeat?
The registered manufacturer of record for NeuroLF Seeat is Positrigo AG.
What is the Primary UDI-DI identifier for NeuroLF Seeat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07649998522045.
What classification code is assigned to this device?
This device is registered under product classification code Z11020480.
Similar Classification Devices (Z11020480)
Other Devices by Positrigo AG
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