Bodenaufbauflansch Poollift / In-ground installation frame (UDI 04260681890383)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The Bodenaufbauflansch Poollift / In-ground installation frame (Model/Catalog Number: K125 BEKA Medicare Pool Lifter 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
- K125 BEKA Medicare Pool Lifter und deren Zubehör
- Product Code / EMDN
- Y093399
- Device Name
- Medicare-Pool-Lift
- Database Sync Date
- 2026-08-09 16:46:36
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 Bodenaufbauflansch Poollift / In-ground installation frame?
The registered manufacturer of record for Bodenaufbauflansch Poollift / In-ground installation frame is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for Bodenaufbauflansch Poollift / In-ground installation frame?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260681890383.
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