MONA EL 200-100, batterie-betrieben / battery-operated (UDI 04260735021350)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The MONA EL 200-100, batterie-betrieben / battery-operated (Model/Catalog Number: K126 BEKA ANA & MONA Pflege-&Versorgungsliegen) 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
- K126 BEKA ANA & MONA Pflege-&Versorgungsliegen
- Product Code / EMDN
- Y1803
- Device Name
- ANA EL 100-80
- Database Sync Date
- 2026-08-09 16:30:09
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 MONA EL 200-100, batterie-betrieben / battery-operated?
The registered manufacturer of record for MONA EL 200-100, batterie-betrieben / battery-operated is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for MONA EL 200-100, batterie-betrieben / battery-operated?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260735021350.
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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