eudamed_udi
Primary ID: 07350181071119
Nordmov Lift E1 (UDI 07350181071119)
Manufactured by Biznord AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nordmov Lift E1 - Primary ID 07350181071119
Device Regulatory Overview
The Nordmov Lift E1 (Model/Catalog Number: NMLE1) is a medical device manufactured by Biznord AB. This product is indexed under FDA Product Code / Category Classification V080502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NMLE1
- Product Code / EMDN
- V080502
- Device Name
- Nordmov Lift
- Database Sync Date
- 2026-08-09 18:20:57
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 Nordmov Lift E1?
The registered manufacturer of record for Nordmov Lift E1 is Biznord AB.
What is the Primary UDI-DI identifier for Nordmov Lift E1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350181071119.
What classification code is assigned to this device?
This device is registered under product classification code V080502.
Similar Classification Devices (V080502)
Other Devices by Biznord AB
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