SecurEline® Buste per la sterilizzazione | Sterilization pouches (UDI +E417203200601)
Manufactured by ELINE S.R.L.
Device Regulatory Overview
The SecurEline® Buste per la sterilizzazione | Sterilization pouches (Model/Catalog Number: 20320060) is a medical device manufactured by ELINE S.R.L.. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20320060
- Product Code / EMDN
- S01010101
- Device Name
- Sterilization pouches
- Database Sync Date
- 2026-08-09 16:29:36
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 SecurEline® Buste per la sterilizzazione | Sterilization pouches?
The registered manufacturer of record for SecurEline® Buste per la sterilizzazione | Sterilization pouches is ELINE S.R.L..
What is the Primary UDI-DI identifier for SecurEline® Buste per la sterilizzazione | Sterilization pouches?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E417203200601.
What classification code is assigned to this device?
This device is registered under product classification code S01010101.
Similar Classification Devices (S01010101)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint