eudamed_udi
Primary ID: 04251816800735
KU-1080/LR (UDI 04251816800735)
Manufactured by AGA Sanitätsartikel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KU-1080/LR - Primary ID 04251816800735
Device Regulatory Overview
The KU-1080/LR (Model/Catalog Number: 48) is a medical device manufactured by AGA Sanitätsartikel GmbH. This product is indexed under FDA Product Code / Category Classification V080699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 48
- Product Code / EMDN
- V080699
- Device Name
- Liege
- Database Sync Date
- 2026-08-09 16:47:01
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 KU-1080/LR?
The registered manufacturer of record for KU-1080/LR is AGA Sanitätsartikel GmbH.
What is the Primary UDI-DI identifier for KU-1080/LR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816800735.
What classification code is assigned to this device?
This device is registered under product classification code V080699.
Similar Classification Devices (V080699)
Other Devices by AGA Sanitätsartikel GmbH
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