eudamed_udi
Primary ID: 04260735020063
SENTA PUR L (UDI 04260735020063)
Manufactured by BEKA-Hospitec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SENTA PUR L - Primary ID 04260735020063
Device Regulatory Overview
The SENTA PUR L (Model/Catalog Number: K121 BEKA Dusch- und Badelifter und deren Zubehöre) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification Y093312 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K121 BEKA Dusch- und Badelifter und deren Zubehöre
- Product Code / EMDN
- Y093312
- Device Name
- EVE!
- Database Sync Date
- 2026-08-09 16:29:19
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 SENTA PUR L?
The registered manufacturer of record for SENTA PUR L is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for SENTA PUR L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260735020063.
What classification code is assigned to this device?
This device is registered under product classification code Y093312.
Similar Classification Devices (Y093312)
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