Vario-Line Spezial 3 EL (UDI 04260735022302)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The Vario-Line Spezial 3 EL (Model/Catalog Number: K101 BEKA Pflege- und Versorgungsliegen und deren Zubehöre) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K101 BEKA Pflege- und Versorgungsliegen und deren Zubehöre
- Product Code / EMDN
- Y1803
- Device Name
- Manipulat 2-HYD
- Database Sync Date
- 2026-08-09 16:46:25
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 Vario-Line Spezial 3 EL?
The registered manufacturer of record for Vario-Line Spezial 3 EL is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for Vario-Line Spezial 3 EL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260735022302.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
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