eudamed_udi
Primary ID: 04061482350249
Haltegriff weiß, 800mm, Rosette weiß (UDI 04061482350249)
Manufactured by Lehnen GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Haltegriff weiß, 800mm, Rosette weiß - Primary ID 04061482350249
Device Regulatory Overview
The Haltegriff weiß, 800mm, Rosette weiß (Model/Catalog Number: CLPESG80WWM) 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
- CLPESG80WWM
- Product Code / EMDN
- Y181806
- Device Name
- Haltegriff glatt 300mm
- Database Sync Date
- 2026-08-09 16:28:52
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 Haltegriff weiß, 800mm, Rosette weiß?
The registered manufacturer of record for Haltegriff weiß, 800mm, Rosette weiß is Lehnen GmbH.
What is the Primary UDI-DI identifier for Haltegriff weiß, 800mm, Rosette weiß?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04061482350249.
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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