eudamed_udi
Primary ID: +E3071157271
E8 24L (UDI +E3071157271)
Manufactured by EURONDA S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for E8 24L - Primary ID +E3071157271
Device Regulatory Overview
The E8 24L (Model/Catalog Number: 115727) is a medical device manufactured by EURONDA S.P.A.. This product is indexed under FDA Product Code / Category Classification Z12011305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 115727
- Product Code / EMDN
- Z12011305
- Device Name
- SSU\E24L2018
- Database Sync Date
- 2026-08-09 16:46:57
Full Regulatory Attributes
đź”’ Token Gated
{
"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 E8 24L?
The registered manufacturer of record for E8 24L is EURONDA S.P.A..
What is the Primary UDI-DI identifier for E8 24L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E3071157271.
What classification code is assigned to this device?
This device is registered under product classification code Z12011305.
Similar Classification Devices (Z12011305)
Other Devices by EURONDA S.P.A.
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