GUDIDData
gudid Primary ID: E3146UUS-206B

OSSEOUS Silicone Sheeting Blue Folios (UDI E3146UUS-206B)

Manufactured by EON MEDITECH PRIVATE LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OSSEOUS Silicone Sheeting Blue Folios - Primary ID E3146UUS-206B

Device Regulatory Overview

The OSSEOUS Silicone Sheeting Blue Folios (Model/Catalog Number: E3146UUS-206B) is a medical device manufactured by EON MEDITECH PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification EPP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
E3146UUS-206B
Product Code / EMDN
EPP
Device Name
"Internal Nasal Splint enhances patient comfort by Allowing nasal breathing while providing support of nasal Septal structure."
Database Sync Date
2026-08-09 09:29:38

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of OSSEOUS Silicone Sheeting Blue Folios?

The registered manufacturer of record for OSSEOUS Silicone Sheeting Blue Folios is EON MEDITECH PRIVATE LIMITED.

What is the Primary UDI-DI identifier for OSSEOUS Silicone Sheeting Blue Folios?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E3146UUS-206B.

What classification code is assigned to this device?

This device is registered under product classification code EPP.

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