eudamed_udi
Primary ID: 04250365214659
Winkelgriff 90° matt gebürstet,links,305x610mm (UDI 04250365214659)
Manufactured by Lehnen GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Winkelgriff 90° matt gebürstet,links,305x610mm - Primary ID 04250365214659
Device Regulatory Overview
The Winkelgriff 90° matt gebürstet,links,305x610mm (Model/Catalog Number: L1012124) is a medical device manufactured by Lehnen GmbH. This product is indexed under FDA Product Code / Category Classification Y181806 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L1012124
- Product Code / EMDN
- Y181806
- Device Name
- Haltegriff glatt 300mm
- Database Sync Date
- 2026-08-09 16:29:37
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 Winkelgriff 90° matt gebürstet,links,305x610mm?
The registered manufacturer of record for Winkelgriff 90° matt gebürstet,links,305x610mm is Lehnen GmbH.
What is the Primary UDI-DI identifier for Winkelgriff 90° matt gebürstet,links,305x610mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250365214659.
What classification code is assigned to this device?
This device is registered under product classification code Y181806.
Similar Classification Devices (Y181806)
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