AVERO Motion / AVERO Motion E (UDI 04260715450422)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The AVERO Motion / AVERO Motion E (Model/Catalog Number: K122 BEKA Pflegebadewannen und deren Zubehör) 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 Pflegebadewannen und deren Zubehör
- Product Code / EMDN
- Y093399
- Device Name
- AVERO Motion
- Database Sync Date
- 2026-08-09 16:46:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AVERO Motion / AVERO Motion E?
The registered manufacturer of record for AVERO Motion / AVERO Motion E is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for AVERO Motion / AVERO Motion E?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260715450422.
What classification code is assigned to this device?
This device is registered under product classification code Y093399.
Similar Classification Devices (Y093399)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint