eudamed_udi
Primary ID: 80572715496936
Pile-UpS (UDI 80572715496936)
Manufactured by Selefar S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pile-UpS - Primary ID 80572715496936
Device Regulatory Overview
The Pile-UpS (Model/Catalog Number: SE-PUS) is a medical device manufactured by Selefar S.r.l.. This product is indexed under FDA Product Code / Category Classification Z12030399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SE-PUS
- Product Code / EMDN
- Z12030399
- Device Name
- Supporto su ruote per pompe d'infusione
- Database Sync Date
- 2026-08-09 16:50:45
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 Pile-UpS?
The registered manufacturer of record for Pile-UpS is Selefar S.r.l..
What is the Primary UDI-DI identifier for Pile-UpS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80572715496936.
What classification code is assigned to this device?
This device is registered under product classification code Z12030399.
Similar Classification Devices (Z12030399)
Other Devices by Selefar S.r.l.
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