eudamed_udi
Primary ID: G15568010
Bein Root Elevator 1 (UDI G15568010)
Manufactured by Nadir & CO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bein Root Elevator 1 - Primary ID G15568010
Device Regulatory Overview
The Bein Root Elevator 1 (Model/Catalog Number: 6801) is a medical device manufactured by Nadir & CO. This product is indexed under FDA Product Code / Category Classification L150301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6801
- Product Code / EMDN
- L150301
- Device Name
- Bein Root Elevator 1
- Database Sync Date
- 2026-08-09 16:46:22
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 Bein Root Elevator 1?
The registered manufacturer of record for Bein Root Elevator 1 is Nadir & CO.
What is the Primary UDI-DI identifier for Bein Root Elevator 1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G15568010.
What classification code is assigned to this device?
This device is registered under product classification code L150301.
Similar Classification Devices (L150301)
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