Wannenverkürzer / Tub shortener (UDI 04260715452372)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The Wannenverkürzer / Tub shortener (Model/Catalog Number: K122 BEKA Zubehöre für Pflegebadewannen) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification Y093399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K122 BEKA Zubehöre für Pflegebadewannen
- Product Code / EMDN
- Y093399
- Device Name
- AVERO Motion
- Database Sync Date
- 2026-08-09 16:29:05
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 Wannenverkürzer / Tub shortener?
The registered manufacturer of record for Wannenverkürzer / Tub shortener is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for Wannenverkürzer / Tub shortener?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260715452372.
What classification code is assigned to this device?
This device is registered under product classification code Y093399.
Similar Classification Devices (Y093399)
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